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5447-96-1

5447-96-1

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5447-96-1 Usage

Physical state

Liquid

Color

Pale yellow

Odor

Characteristic

Reactivity

Reactive

Toxicity

Toxic

Uses

a. Reagent in organic synthesis
b. Production of pharmaceuticals
c. Production of agrochemicals
d. Solvent in various chemical processes

Hazardous nature

Yes

Safety precautions

a. Potential for skin and eye irritation
b. Potential for respiratory and digestive tract problems upon exposure
c. Appropriate handling and safety measures required

Check Digit Verification of cas no

The CAS Registry Mumber 5447-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5447-96:
(6*5)+(5*4)+(4*4)+(3*7)+(2*9)+(1*6)=111
111 % 10 = 1
So 5447-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C3H6BrNO2/c1-2-3(4)5(6)7/h3H,2H2,1H3

5447-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-1-nitropropane

1.2 Other means of identification

Product number -
Other names 1-bromonitropropane

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:5447-96-1 SDS

5447-96-1Relevant articles and documents

-

Erickson,A.S.,Kornblum,N.

, p. 3764 - 3765 (1977)

-

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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