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595-44-8

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595-44-8 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong, pungent

Uses

a. Intermediate in the synthesis of pharmaceuticals and organic compounds
b. Solvent
c. Production of pesticides

Toxicity

Toxic and harmful if swallowed, inhaled, or absorbed through the skin

Health hazards

Can cause irritation to the respiratory system and skin

Classification

Hazardous substance

Handling and storage

Requires careful handling and storage

Check Digit Verification of cas no

The CAS Registry Mumber 595-44-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 595-44:
(5*5)+(4*9)+(3*5)+(2*4)+(1*4)=88
88 % 10 = 8
So 595-44-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H5Cl2NO2/c1-2-3(4,5)6(7)8/h2H2,1H3

595-44-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-Dichloro-1-nitropropane

1.2 Other means of identification

Product number -
Other names 1,1-Dichlor-1-nitropropan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:595-44-8 SDS

595-44-8Downstream Products

595-44-8Relevant articles and documents

Electrooxidative coupling of salts of nitro compounds with halide, nitrite, cyanide, and phenylsulfinate anions

Ilovaisky,Merkulova,Ogibin,Nikishin

, p. 1585 - 1592 (2007/10/03)

Electrolysis of salts of primary and secondary nitro compounds (nitroethane, 1- and 2-nitropropanes, nitrocyclohexane, and nitrocycloheptane) in the presence of excess halide, nitrite, cyanide, and phenylsulfinate anions under undivided and divided amperostatic electrolysis conditions in a two-phase medium (CH2Cl2/H2O) produces geminal nitrohalides (35-85% yields), dinitro compounds (15-51%), nitronitriles (6-27%), and nitrosulfones (50-70%). The salts of secondary nitro compounds form the products of oxidative coupling with halide and phenylsulfinate anions under the undivided electrolysis conditions. In all other cases, divided electrolysis is required.

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