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Merck
CN

147338

苄烯丙二腈

98%

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线性分子式:
C6H5CH=C(CN)2
化学文摘社编号:
分子量:
154.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-283-6
MDL number:
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产品名称

苄烯丙二腈, 98%

InChI key

WAVNYPVYNSIHNC-UHFFFAOYSA-N

InChI

1S/C10H6N2/c11-7-10(8-12)6-9-4-2-1-3-5-9/h1-6H

SMILES string

N#C\C(=C/c1ccccc1)C#N

assay

98%

mp

83-85 °C (lit.)

functional group

nitrile
phenyl

Quality Level

Application

苄叉丙二腈用于基于荧光的测定溶液中可溶性甲烷单加氧酶的活性

General description

亚苄基马来腈与伯烷基胺发生快速、无催化剂的气固反应生成 N -亚苄基胺 。它与氯化正辛基和正癸基锆发生加成反应 。它是可溶性甲烷单加氧酶的潜在底物

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A R Miller et al.
Applied microbiology and biotechnology, 58(2), 183-188 (2002-03-06)
A fluorescence-based assay was developed to estimate soluble methane monooxygenase (sMMO) activity in solution. Whole cells of Methylosinus trichosporium OB3b expressing sMMO were used to oxidize various compounds to screen for fluorescent products. Of the 12 compounds tested, only coumarin
Liqi Shi et al.
Chemical communications (Cambridge, England), 50(7), 872-874 (2013-12-04)
A new rapid and catalyst-free solid/vapor reaction between benzylidenemalonate/benzylidenemalononitrile and primary alkyl amines was found. With these as sensory units of fluorescent polymers, probes for primary amine vapor with high sensitivity and selectivity were developed.
Yuanhong Liu et al.
The Journal of organic chemistry, 67(20), 7019-7028 (2002-10-02)
Direct addition of alkylzirconocenes to activated alkenes was found, for the first time. Octyl- and decylzirconocene chloride reacted with benzylidenemalononitrile to give the corresponding addition products after hydrolysis in 86% and 79% yield, respectively. Zirconacyclopentanes showed a similar reactivity toward

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