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37675-31-3

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37675-31-3 Usage

Physical state

Colorless liquid

Odor

Strong, irritating

Primary use

Synthesis of other organic chemicals

Intermediate in production

Pharmaceuticals and agricultural products

Additional uses

Pesticide, flame retardants, and plastics

Hazard classification

Classified as a hazardous substance

Health hazards

Causes irritation to skin, eyes, and respiratory system

Environmental impact

Potentially harmful to aquatic life if released into the environment

Safety precautions

Handle with caution to minimize exposure and environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 37675-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,7 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37675-31:
(7*3)+(6*7)+(5*6)+(4*7)+(3*5)+(2*3)+(1*1)=143
143 % 10 = 3
So 37675-31-3 is a valid CAS Registry Number.

37675-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-bromo-3-chloroprop-1-ene

1.2 Other means of identification

Product number -
Other names 1t-bromo-3-chloro-propene

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:37675-31-3 SDS

37675-31-3Relevant articles and documents

3-Chloro-1-lithiopropene, a functional organolithium reagent, and its reactions with alkylboronates to give 3-alkylprop-1-en-3-ols

Smith, Keith,Elliott, Mark C.,Jones, D. Heulyn

, p. 9526 - 9531 (2013/10/08)

The reagent 3-chloro-1-lithiopropene (4) can be generated by treating 1-bromo-3-chloropropene with t-BuLi. It is unstable but if generated at low temperature in the presence of alkylboronic esters, such as 3, is trapped in situ to give rearrangement products 2, which on oxidation give 3-alkylprop-1-en-3-ols in good yields. The reaction works for primary, secondary, benzylic, and even tertiary alkylboronic esters, providing allylic alcohols bearing almost any alkyl group available using organoborane chemistry and incorporating all features of such groups.

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