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.
signalword
Danger
hcodes
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
新产品
此项目有
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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