P31205
苯丙炔酸
99%
别名:
苯基丙炔酸
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关于此项目
线性分子式:
C6H5C≡CCOOH
化学文摘社编号:
分子量:
146.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-285-8
Beilstein/REAXYS Number:
742587
MDL number:
Assay:
99%
Form:
crystals
InChI key
XNERWVPQCYSMLC-UHFFFAOYSA-N
InChI
1S/C9H6O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-5H,(H,10,11)
SMILES string
OC(=O)C#Cc1ccccc1
assay
99%
form
crystals
Quality Level
storage temp.
2-8°C
Application
苯丙酸可以：
- 在三氟化硼 · 二乙基醚的存在下与 2- 叔 -丁氧基吡啶反应生成相应的 叔 -丁酯。
- 与芳基卤化物如 对 -氯碘苯和 1-氯-4-碘苯发生脱羧偶联。
- 发生卤代脱羧反应生成 1-卤代炔。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Neil R McIntyre et al.
Journal of enzyme inhibition and medicinal chemistry, 31(4), 551-562 (2015-05-30)
Peptidylglycine α-amidating monooxygenase (PAM) is a bifunctional enzyme that catalyzes the final reaction in the maturation of α-amidated peptide hormones. Peptidylglycine α-hydroxylating monooxygenase (PHM) is the PAM domain responsible for the copper-, ascorbate- and O2-dependent hydroxylation of a glycine-extended peptide.
M Zieliński et al.
Isotopes in environmental and health studies, 37(3), 239-252 (2002-04-02)
13C kinetic isotope effect (KIE) in the decarboxylation of phenylpropiolic acid (PPA) in tetralin medium (Tn) has been determined at 409-432 K and found to be of magnitude similar to the 13C KIE observed in the decarboxylation of malonic acid
Rocío Gómez-Vásquez et al.
Annals of botany, 94(1), 87-97 (2004-05-18)
Control of diseases in the key tropical staple, cassava, is dependent on resistant genotypes, but the innate mechanisms are unknown. The aim was to study phenylpropanoids and associated enzymes as possible defence components. Phenylalanine ammonia-lyase (PAL), phenylpropanoids and peroxidases (POD)
Jill Wood et al.
Bioorganic & medicinal chemistry letters, 16(18), 4965-4968 (2006-06-30)
A series of 4,5-disubstituted cis-pyrrolidinones was investigated as inhibitors of 17beta-HSD II for the treatment of osteoporosis. Biochemical data for several compounds are given. Compound 42 was selected as the lead candidate.
Jan Schwarzbauer et al.
Water research, 39(19), 4735-4748 (2005-11-11)
Detailed gas chromatographic-mass spectrometric analyses applied to eight Rhine river water samples constituted a comprehensive characterization of the low molecular weight organic contamination. Within the group of predominant anthropogenic contaminants, only a few compounds were characterized as frequently detected or
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