• Bulletin of the Korean Chemical Society
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• 제13권5호
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• pp.547-550
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• 1992

The oxidation of benzaldehyde, 3,4-dimethoxy benzaldehyde, p-methoxy benzaldehyde, m-$NO_2$-benzaldehyde, and m-chlorobenzaldehyde by pyridinium chlorochromate (Corey's reagent) are reported. Michaelis-Menten behaviour is observed. The rate determining step appears to be the decomposition of a complex of benzaldehyde with PCC either through a loss of $H^+$ or $H^-$ ions.

• 약학회지
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• 제6권1호
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• pp.5-7
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• 1962

Like the condensation reaction of general aldehyde, that of benzaldehyde with semicarbazide also depends upon the concentration of carbonium ion that is produced by hydrogen ion. The lower pH value is the facility of the formation of carbonium ion in the condensation reaction, while the reactivity of semicarbazide as a reactant is reduced. In this paper, therefore we want to find out the optimum pH value in the condensation reaction of benzaldehyde with semicarbazide. This optimum pH value was determined by using the simple paper-chromatographic method. According to the result of this experiment, the condensation reaction between benzaldehyde and semicarbazide reacts with its highest point at 3.5pH value. It seems clear that at this point the benzaldehyde acquires the most suitable amount of carbonium ion for the condensation reaction with semicarbazide, and the semicarbazide also has the optimum reactivity.

• Bulletin of the Korean Chemical Society
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• 제17권2호
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• pp.128-131
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• 1996

From Raman spectra, the ${\nu}g$C=O frequencies of 4-substituted benzaldehydes were found to correlate with the ${\sigma}_p$ values of the 4-x atom or group as well as the acceptor number (AN) values of solvents. In various solvents, the ${\nu}g$C=O frequency of benzaldehyde decreased upon the increase of benzaldehyde concentration. This shift was mainly due to the hydrogen bonding between the carbonyl oxygen and/or aldehydic proton of benzaldehyde and the solvent molecules. Over the 1-80 volume % change, the ${\nu}g$C=O frequency of benzaldehyde down shifted from 1709.4 $cm^{-1}$ to 1700.2 $cm^{-1}$ in CCl4 solution and from 1703.0 $cm^{-1}$ to 1698.0 $cm^{-1}$ in $C_2H_5OH$ solution. This is due to the fact that hydrogen bonding between the benzaldehyde and C2H5OH was much stronger than that between the benzaldehyde and the other solvents.

• Bulletin of the Korean Chemical Society
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• 제13권2호
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• pp.179-183
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• 1992

A stable solid new inclusion complex with benzaldehyde and $permethyl-\beta-cyclodextrin$ was obtained by recrystallization method. The structure of the $benzaldehyde-permethyl-\beta-cyclodextrin$ inclusion complex in the solid and solution state have been studied by UV, IR, $^1H-NMR$, $^{13}C-NMR$ and FAB-mass spectroscopy.

• Journal of Microbiology
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• 제37권4호
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• pp.224-228
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• 1999

Benzaldehyde dehydrogenase (BZDH), an enzyme involved in the degradation of toluene and xylenes, is encoded by the phnN gene of Pseudomonas sp. strain DJ77. We determined the nucleotide sequence of a DNA fragment of 1,803 base pairs which included the phnN gene. The fragment contained an open reading frame of 1,506 base pairs to accommodate th 55 kDa sized enzyme encoding BZDH. The enzyme efficiently oxidized benzaldehyde, salicylaldehyde, m-tolualdehyde and ps-tolualdehyde.

• Bulletin of the Korean Chemical Society
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• 제20권3호
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• pp.307-313
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• 1999

2,4-Di-(2'-vinyloxyethoxy)benzylidenemalononitrile (la), methyl 2,4-di-(2'-vinyloxyethoxy)benzylidenecyanoacetate (lb), 3,4-di-(2'-vinyloxyethoxy)benzylidene malononitrile (2a), methyl 3,4-di-(2'-vinyloxyethoxy)benzylidenecyanoacetate (2b), 2,5-di-(2'-vinyloxyethoxy)benzylidenemalononitrile (3a), methyl 2,5-di-(2'-vinyloxyethoxy)benzylidenecyanoacetate (3b), 2,3-di-(2'-vinyloxyethoxy)benzylidenemalononitrile (4a), and methyl 2,3-di-(2'-vinyloxyethoxy)benzylidenecyanoacetate (4b) were prepared by the condensation of 2,4-di-(2'-vinyloxyethoxy)benzaldehyde, 3,4-di-(2'-vinyloxyethoxy)benzaldehyde, 2,5-di-(2'-vinyloxyethoxy) benzaldehyde, and 2,3-di-(2'-vinyloxyethoxy)benzaldehyde with malononitrile or methyl cyanoacetate, respectively. Trifunctional divinyl ether monomers 1-4 were polymerized readily with boron trifluoride etherate as a cationic initiator to give optically transparent swelling poly(vinyl ethers) 5-8 havina oxybenzylidenemalononitrile and oxycyanocinnamate, which is presumably effective chromophore for second-order nonlinear optical applications. Polymers 5-8 were not soluble in common organic solvents such as acetone and DMSO due to crosslinking. Polymers 5-8 showed a thermal stability up to 300 ℃ in TGA thermograms, which is acceptable for electrooptic device applications.

• Toxicological Research
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• 제11권2호
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• pp.279-288
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• 1995

To apply the serum xanthine oxidase (XO) determining for the index of the toluene intoxication, the serum XO activity was compared with the other parameters, the activities of serum alanine aminotransferase(ALT), aspartate aminotransferase(AST), 5'-nucleotidase(5'-NT), alkaline phosphatase(ALP), guanase(GDA) and $\gamma$-gIutamyl transpeptidase(T-GTP). Concomitantly, the cause of increased level of serum XO was clarified in the present experimental conditions. Although the other serum enzyme activities, ALT, AST, 5'-NT, ALP, GDA and $\gamma$-GTP were respectively not found to be different between control group and toluene-treated group, the serum XO activity in toluene-treated group showed the higher levels than that in the control group. These suggested that the determination of serum XO activity could be used for monitoring the intoxication of toluene. On the other hand, the activities of XO both in the serum and liver were higher in toluene-treated or benzaldehyde-treated rats than those in each control group. In the pooled liver XO from each group, toluene-treated or benzaldehyde-treated group showed the higher $V_{max}$ value than the control group, whereas no changes were observed in liver XO activities between the control liver specimen and that preincubated with bertzaldehyde in vitro. The present results indicate that the increased level of XO in toluene-treated rats is due to the result of enzyme protein induction in liver cell by the benzaldehyde metabolized from toluene. All the more, the benzaldehyde may be acted as a substrate for XO, since the benzaldehyde induced the increased activity of both liver and serum XO, and no changes were found in purine catabolite, uric acid in serum or urine and liver purine catabolizing enzymes, adenosine deaminase, GDA, uricuse except XO in toluene-treated rats.

• 한국식품과학회지
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• 제14권4호
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• pp.315-323
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• 1982

설탕용액중 benzaldehyde의 의사 2성분계 확산계수를 농도 및 온도를 변화시켜 측정하여 이론식과 비교 검토한 결과 다음과 같은 결론을 얻어 내었다. 1. $20{\sim}40^{\circ}C$의 일정한 온도에서 설탕용액중 benzaldehyde의 확산계수는 점도의 -0.82승에 비례하며 이것은 매질이나 확산되는 물질에 따라 차이가 생긴다. 2. 일정한 온도에서 적어도 두 개 이상의 농도에서 확산계수를 알 수 있다면 Tang-Himmelblau식을 이용하여 Wilke-Chang식 보다 정확하게 확산계수를 예측할 수 있으며 설탕용액에서 ${\varepsilon}=0.2$라 놓을수 있고, 설탕의 회합인자, ${\varphi}_s=2$라 놓을수 있다. 또 Bird 등에 의한 effective diffusivity는 고점도 범위에서는 사용할 수 없다. 3. 염화칼륨을 이용하여 격막 cell 방법으로 cell 상수를 결정할 때 수용액중 염화캄륨의 확산계수가 농도의 영향을 적게 받는 농도범위, 즉 0.05N 이상에서 측정하는 것이 좋으며 온도의 영향은 크지 않으나 상온 부근의 저온에서 측정하는 것이 좋다.

• 한국잡초학회지
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• 제30권3호
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• pp.191-198
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• 2010

본 연구의 목적은 정유에 함유되어 있는 살초활성물질을 탐색하여 제초제 개발을 위한 선도 화합물을 발굴하는데 있었다. Amyris(Amyris balsamifera), cajuput (Melaleuca cajeputi), geranium(Pelargonium graveolens), lavender(Lavendula spp.), mandarin(Citrus reticulata), pine(Pinus spp.) 및 rosemary(Rosmarius officinale) 정유에 대한 살초력을 유채(Brassica napus)를 대상으로 in vitro에서 수행한 결과, cajuput 정유의 살초력이 가장 높았다($GR_{50}$ 값, $425{\mu}g\;g^{-1}$). Cajuput 정유에 함유되어 있는 주된 생리활성물질들은 eucalyptol 37,2%, ${\alpha}$-terpineol 11.6%, benzaldehyde 5.2%, linalool 4.1%, ${\alpha}$-pinene 2.5%, ${\beta}$-pinene 2.4%이었으며, 이들 생리활성물질의 살초력($GR_{50}$ 값)은 각각 2,731, 500, 50, 372, 4,363, $4,671{\mu}g\;g^{-1}$이었다. Benzaldehyde의 살초력은 기 보고된 eucalyptol (1,8-cineole)과 ${\alpha}$-pinene보다 높았으므로 향후 새로운 제초제 개발을 위한 선도화합물로 활용될 수 있을 것이라 판단된다. Cajuput 정유와 이에 함유되어 있는 가장 높은 살초력을 보였던 benzaldehyde를 80kg $ha^{-1}$ 토양처리하였을 때에는 그 어떠한 살초효과도 관찰할 수 없었으나, 경엽처리 하였을 때에는 화본과 잡초인 수수, 돌피, 바랭이는 100% 고사되었다. 그러나 살초효과는 20kg $ha^{-1}$ 이하에서는 전혀 나타나지 않았는데 이는 cajuput 정유와 benzaldehyde의 높은 휘발성 때문인 것으로 추론된다. 본 연구의 결과 cajuput 정유의 살초효과는 높은 약량에서만 나타났으므로 약량저감을 위한 처리시기 재설정과 살초력을 높일 수 있는 제형개발이 요구된다.

• Bulletin of the Korean Chemical Society
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• 제23권2호
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• pp.286-290
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• 2002

Hydrogen atom production channels from photodissociation of benzene, phenylacetylene, and benzaldehyde at 243 nm have been investigated by detecting H atoms using two photon absorption at 243.2 nm and induced fluorescence at 121.6 nm. Translational energies of the H atoms were measured by Doppler broadened H atom spectra. By absorption of two photons at 243 nm, the H atoms are statistically produced from benzene and phenylacetylene whereas the H atoms from the aldehyde group in benzaldehyde are produced from different pathways. The possible dissociation mechanisms are discussed from the measured translational energy releases.