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563-97-3

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563-97-3 Usage

Physical state

Colorless to light yellow liquid

Odor

Strong, pungent

Uses

a. Reagent in organic synthesis
b. Production of pharmaceuticals
c. Production of dyes
d. Production of agrochemicals
e. Manufacture of specialty chemicals
f. Solvent in industrial processes

Toxicity

Highly toxic if ingested, inhaled, or absorbed through the skin

Safety precautions

Proper handling and storage required

Hazard classification

Severe fire and explosion hazard

Storage and handling

Special procedures required to prevent accidents

Check Digit Verification of cas no

The CAS Registry Mumber 563-97-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 563-97:
(5*5)+(4*6)+(3*3)+(2*9)+(1*7)=83
83 % 10 = 3
So 563-97-3 is a valid CAS Registry Number.

563-97-3SDS

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-bromo-1-nitroethane

1.2 Other means of identification

Product number -
Other names 1-Brom-1-nitro-aethan

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:563-97-3 SDS

563-97-3Relevant articles and documents

-

Fetell,A.I.,Feuer,H.

, p. 1238 - 1241 (1978)

-

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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