116025
扁桃腈
technical grade
别名:
α-氰基苄醇, 杏仁腈, 苯甲氰醇
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关于此项目
线性分子式:
C6H5CH(OH)CN
化学文摘社编号:
分子量:
133.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-532-7
Beilstein/REAXYS Number:
2207122
MDL number:
refractive index
n20/D 1.530 (lit.)
bp
170 °C (lit.)
solubility
alcohol: freely soluble, chloroform: freely soluble, diethyl ether: freely soluble
density
1.117 g/mL at 25 °C (lit.)
functional group
hydroxyl, nitrile, phenyl
InChI key
NNICRUQPODTGRU-UHFFFAOYSA-N
InChI
1S/C8H7NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8,10H
SMILES string
OC(C#N)c1ccccc1
grade
technical grade
Application
Mandelonitrile has been used to extract mandeloamide by the nitrilase variants.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
206.6 °F - closed cup
flash_point_c
97 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Olga Sosedov et al.
Applied microbiology and biotechnology, 98(4), 1595-1607 (2013-05-23)
The nitrilase from Pseudomonas fluorescens EBC191 was modified by introducing random mutations via error-prone PCR techniques in order to obtain nitrilase variants, which form increased amounts of mandeloamide from racemic mandelonitrile. A screening system was established and experimentally optimized, which
Y Leong Yeow et al.
Journal of biotechnology, 111(1), 31-39 (2004-06-16)
The progress curves of conversion of racemic-mandelonitrile (R-MN) at different concentrations to benzaldehyde (BA) and hydrogen cyanide (HCN), catalyzed by S-hydroxynitrile lyase from Hevea brasiliensis, together with the enantiomeric excess curves of R-MN are converted into individual progress curves of
Laboratory evolved biocatalysts for stereoselective syntheses of substituted benzaldehyde cyanohydrins.
Zhibin Liu et al.
Chembiochem : a European journal of chemical biology, 9(1), 58-61 (2007-12-07)
A biocatalytic Henry reaction--the hydroxynitrile lyase from Hevea brasiliensis also catalyzes nitroaldol reactions.
Thomas Purkarthofer et al.
Angewandte Chemie (International ed. in English), 45(21), 3454-3456 (2006-04-25)
D H Sreenivasa Rao et al.
Applied biochemistry and biotechnology, 193(2), 560-576 (2020-10-13)
Enantiopure β-nitroalcohols are versatile intermediates used in the synthesis of important pharmaceuticals and chiral synthons. In this article, immobilized Arabidopsis thaliana HNL (AtHNL)-catalyzed preparation of (S)-β-nitroalcohols from their racemic mixtures via retro-Henry reaction was studied. AtHNL used in biocatalysis was
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