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About This Item
線性公式:
CH3CH(C6H5)CH2CHO
CAS號碼:
分子量：:
148.20
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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推薦產品
化驗
97%
形狀
liquid
折射率
n20/D 1.5179 (lit.)
bp
93-94 °C/16 mmHg (lit.)
密度
0.997 g/mL at 25 °C (lit.)
官能基
aldehyde
phenyl
SMILES 字串
[H]C(=O)CC(C)c1ccccc1
InChI
1S/C10H12O/c1-9(7-8-11)10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3
InChI 密鑰
MYHGOWDLVRDUFA-UHFFFAOYSA-N
相關類別
應用
3-Phenylbutyraldehyde was used as a reactant to study the kinetics of the reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G[1].
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
206.6 °F - closed cup
閃點（°C）
97.00 °C - closed cup
個人防護裝備
Eyeshields, Gloves
Holger Bühler et al.
Chembiochem : a European journal of chemical biology, 6(4), 711-717 (2005-04-07)
The influence of Trp128-substituted mutants of the hydroxynitrile lyase from Manihot esculenta (MeHNL) on the stereoselectivity of MeHNL-catalyzed HCN additions to aldehydes with stereogenic centers, which yield the corresponding cyanohydrins, is described. In rac-2-phenylpropionaldehyde (rac-1) reactions, wild-type (wtMeHNL) and all
G M Raner et al.
Journal of inorganic biochemistry, 81(3), 153-160 (2000-10-29)
The reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G results in the covalent modification of the heme cofactor of this monooxygenase. Analysis of the resulting heme by electronic absorption spectrophotometry indicates that the reaction in the BM3
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