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816-21-7

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816-21-7 Usage

Type of compound

Brominated ketone

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Physical state

Colorless liquid

Odor

Strong

Flammability

Highly flammable

Health hazards

Strong irritant to skin, eyes, and respiratory system

Precaution

Exposure should be avoided

Application

Production of fine chemicals

Role in organic synthesis

Important building block

Additional use

Reagent in various chemical reactions

Specific reactions

Synthesis of heterocycles and complex organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 816-21-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 816-21:
(5*8)+(4*1)+(3*6)+(2*2)+(1*1)=67
67 % 10 = 7
So 816-21-7 is a valid CAS Registry Number.

816-21-7SDS

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 1,3-dibromopentan-2-one

1.2 Other means of identification

Product number -
Other names 1,3-Dibromo-2-pentanone

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:816-21-7 SDS

816-21-7Downstream Products

816-21-7Relevant articles and documents

Formation of α-iminoketones and α-diimines versus Favorskii rearrangement products from the reaction of α,α′-dibromoketones and primary amines

De Kimpe, Norbert,D'Hondt, Luc,Mones, Luc

, p. 3183 - 3208 (2007/10/02)

The reaction of aliphatic acyclic α,α'-dibromoketones with primary amines gave rise to α-iminoketones and α-diimines. Both reaction products could be selectively obtained under appropriate reaction conditions. Sterically hindered α,α-dibromoketones did no

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