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1,1-dibromo-1-nitro-propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31253-12-0

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31253-12-0 Usage

Physical state

Colorless to yellow liquid

Odor

Strong, pungent

Primary use

Reagent in chemical synthesis

Applications

Production of pharmaceuticals, agricultural chemicals, dyes, and other organic compounds

Toxicity

Toxic if ingested or inhaled

Health effects

Prolonged exposure can cause irritation to the respiratory system and skin

Carcinogenicity

Potential carcinogen

Mutagenicity

Potential mutagen

Regulation

Regulated and controlled in many jurisdictions due to hazardous properties

Check Digit Verification of cas no

The CAS Registry Mumber 31253-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,2,5 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 31253-12:
(7*3)+(6*1)+(5*2)+(4*5)+(3*3)+(2*1)+(1*2)=70
70 % 10 = 0
So 31253-12-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H5Br2NO2/c1-2-3(4,5)6(7)8/h2H2,1H3

31253-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dibromo-1-nitropropane

1.2 Other means of identification

Product number -
Other names 1,1-Dibrom-1-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:31253-12-0 SDS

31253-12-0Downstream Products

31253-12-0Relevant academic research and scientific papers

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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