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Merck

115959

Sigma-Aldrich

苯甲酰氰

98%

别名:

苯甲酰腈

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About This Item

线性分子式:
C6H5COCN
CAS号:
分子量:
131.13
Beilstein:
1072101
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

形狀

solid

bp

206 °C (lit.)

mp

28-31 °C (lit.)

密度

1.106 g/mL at 25 °C (lit.)

官能基

ketone
nitrile
phenyl

SMILES 字串

O=C(C#N)c1ccccc1

InChI

1S/C8H5NO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H

InChI 密鑰

GJQBHOAJJGIPRH-UHFFFAOYSA-N

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一般說明

用苯甲酰氰化物研究苯甲酰氰化物在乙腈、N,N-二甲基甲酰胺和乙腈中的还原机理 。它经过 红球菌 CCZU10-1水解形成苯甲酰甲酸

應用

氨基化合物的选择性酰化反应试剂。

相關產品

象形圖

Skull and crossbones

訊號詞

Danger

危險聲明

防範說明

危險分類

Acute Tox. 2 Oral

儲存類別代碼

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

183.2 °F - closed cup

閃點(°C)

84 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Synthesis, 433-433 (1993)
Weisi Xiong et al.
Biotechnology letters, 37(8), 1703-1709 (2015-04-22)
To develop a biphasic system for use in plant tissue-mediated biotransformations to overcome the low water solubilities of substrates and inhibitory effects of products. Commonly-used organic solvents and ionic liquid were assayed using the biphasic system to reduce water-insoluble benzoyl
Yi Xu et al.
Journal of virology, 92(11) (2018-03-09)
Translational readthrough of the stop codon of the capsid protein (CP) open reading frame (ORF) is used by members of the Luteoviridae to produce their minor capsid protein as a readthrough protein (RTP). The elements regulating RTP expression are not
Petar I Penev et al.
Genome biology and evolution, 12(10), 1694-1710 (2020-08-14)
The ribosome's common core, comprised of ribosomal RNA (rRNA) and universal ribosomal proteins, connects all life back to a common ancestor and serves as a window to relationships among organisms. The rRNA of the common core is similar to rRNA
Norma A Macías-Ruvalcaba et al.
The Journal of organic chemistry, 72(2), 589-594 (2007-01-16)
The mechanism of reduction of benzoyl cyanide, 6, p-methoxybenzoyl cyanide, 7, and p-chlorobenzoyl cyanide, 8, has been studied in acetonitrile (6 and 7), N,N-dimethylformamide (6), and acetonitrile containing water (all three compounds). The reaction proceeds by initial reduction to form

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