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Merck
CN

143081

二氯代苯胩

98%

别名:

N-二氯亚甲苯胺

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线性分子式:
C6H5N=CCl2
化学文摘社编号:
分子量:
174.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-735-0
MDL number:
Assay:
98%
Form:
liquid
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InChI key

TTWWZVGVBRPHLE-UHFFFAOYSA-N

InChI

1S/C7H5Cl2N/c8-7(9)10-6-4-2-1-3-5-6/h1-5H

SMILES string

Cl\C(Cl)=N\c1ccccc1

assay

98%

form

liquid

refractive index

n20/D 1.571 (lit.)

bp

103-106 °C/30 mmHg (lit.)

density

1.265 g/mL at 25 °C (lit.)

functional group

chloro

storage temp.

2-8°C

Application

Phenyl isocyanide dichloride was used in the synthesis of 5-halo-1-phenyltetrazoles.

Biochem/physiol Actions

Phenyl isocyanide dichloride exhibits spectral interactions with cytochrome P-450 from mouse hepatic microsomes.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

174.2 °F - closed cup

flash_point_c

79 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

Lot/Batch Number

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G A Beumel et al.
General pharmacology, 16(3), 193-197 (1985-01-01)
The binding of isocyanides and the metabolites of piperonyl butoxide (PBO) to reduced cytochrome P-450 in intact microsomes gives rise to the type III optical difference spectrum which is characterized by two pH dependent peaks in the Soret region. Each
5-Halo-1-phenyltetrazoles.
Collibee WL, et al.
The Journal of Organic Chemistry, 60(2), 468-469 (1995)
G A Beumel et al.
General pharmacology, 16(3), 189-192 (1985-01-01)
The spectral interactions of a number of isocyanides with cytochrome P-450 were investigated. An interaction between the hydrophobic nature of the side chain and the spectral interaction was apparent. The concentration of the isocyanide affected the stability of the complex.

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