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1,3-dichloro-2-(chloromethyl)-2-nitropropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79437-10-8

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79437-10-8 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong

Primary use

Solvent in industrial applications

Additional use

Starting material in the synthesis of pharmaceuticals and agrochemicals

Environmental impact

Highly toxic to aquatic organisms

Human health effects

Can cause skin and eye irritation

Genetic effects

Known mutagen

Risk

Potential risk to human health and the environment if not handled and disposed of properly

Check Digit Verification of cas no

The CAS Registry Mumber 79437-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,3 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79437-10:
(7*7)+(6*9)+(5*4)+(4*3)+(3*7)+(2*1)+(1*0)=158
158 % 10 = 8
So 79437-10-8 is a valid CAS Registry Number.

79437-10-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dichloro-2-(chloromethyl)-2-nitropropane

1.2 Other means of identification

Product number -
Other names 1,3-Dichlor-2-chlormethyl-2-nitro-propan

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:79437-10-8 SDS

79437-10-8Relevant academic research and scientific papers

Modulating the propeller-like shape of a tripodal C(CH2PPh2)3 fragment by the size of the substituent at the pivotal carbon atom in macrobicyclic tri-λ5-phosphazenes

Alajarín, Mateo,López-Leonardo, Carmen,Berná, José

, p. 4450 - 4458 (2008/02/03)

The chiral macrobicyclic tri-λ5-phosphazenes formed by tripod-tripod coupling of tris(3-azidobenzyl)amines and 1,1,1-tris[(diphenylphosphino)methyl]methanes present helical topologies as a result of combining two propeller-shaped tripodal fragm

PRODUCTION OF CYCLIC SULFITES AND THEIR TRANSFORMATION INTO SUBSTITUTED TRI(CHLOROMETHYL)METHANES

Bolotov, A. A.,Rodin, A. A.,V'yunov, K. A.,Ginak, A. I.,Sarkisov, Yu. S.

, p. 1812 - 1819 (2007/10/02)

The production of cyclic sulfites from trihydric alcohols and their conversion into chlorides by the action of DMFA-SOCl2 complex are described.By PMR and IR spectroscopy it was shown that cyclic sulfites exist preferentially in the chair conformation with the axial orientation of the S=O bond.It was established that the chlorides are formed in two parallel paths, i.e. directly from trihydric alcohols and their cyclic sulfites.

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