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53535-68-5

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53535-68-5 Usage

Physical State

Clear, colorless liquid

Odor

Pungent

Primary Uses

Intermediate in the production of pharmaceuticals and agrochemicals

Secondary Uses

Reagent in the synthesis of various organic compounds, solvent, and in chemical research

Toxicity

Toxic if ingested or inhaled

Health Hazards

Causes irritation to the skin, eyes, and respiratory system

Safety Precautions

Handle with caution, store and handle in a well-ventilated area away from heat and open flames

Flammability

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 53535-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53535-68:
(7*5)+(6*3)+(5*5)+(4*3)+(3*5)+(2*6)+(1*8)=125
125 % 10 = 5
So 53535-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H22N2O2S/c1-12(2,3)14(13-16)11(17-4)9-7-5-6-8-10(9)15/h11,15H,5-8H2,1-4H3

53535-68-5SDS

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 1-bromo-3-chloropropan-2-one

1.2 Other means of identification

Product number -
Other names 1-Bromo-3-chloro-2-propanone

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:53535-68-5 SDS

53535-68-5Relevant articles and documents

PROCESS FOR PREPARIING 1,3-DIBROMOACETONE, 1-3-DICHLOROACETONE AND EPICHLOROHYDRIN

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Page/Page column 13-14, (2008/06/13)

A process for preparing 1,3-dibromoacetone, 1-3-dichloroacetone and epichlorohydrin which comprises: (a) reacting acetone with 2 moles of bromine to make a mixture of brominated acetone derivatives and byproduct hydrogen bromide; (b) equilibrating the mixture of brominated acetone derivatives and hydrogen bromide to produce 1,3-dibromoacetone as the major product; (c) crystallizing the 1,3-dibromoacetone; and (d) isolating the 1,3-dibromoacetone. The process may further include the steps of (e) reacting the 1,3-dibromoacetone with a chloride source to produce 1,3-dichloroacetone; (f) hydrogenating the isolated 1,3-dichloroacetone to produce 1,3-dichlorohydrin; and (g) cyclizing the 1,3-dichlorohydrin with a base to produce epichlorohydrin.

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