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34181-74-3

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34181-74-3 Usage

Chemical Structure

A complex mixture of polychlorinated compounds

Usage

Pesticide

Toxicity

Highly toxic

Environmental Persistence

Long-lasting in the environment

Banned in many countries

Yes, due to its harmful effects

Health Effects

Can cause damage to the liver, immune system, and reproductive system

Carcinogenic Potential

Considered to be a potential carcinogen

Efforts to phase out

Yes, due to its harmful effects

Cleanup of contaminated sites

Ongoing efforts to clean up sites contaminated with toxaphene

Check Digit Verification of cas no

The CAS Registry Mumber 34181-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,8 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 34181-74:
(7*3)+(6*4)+(5*1)+(4*8)+(3*1)+(2*7)+(1*4)=103
103 % 10 = 3
So 34181-74-3 is a valid CAS Registry Number.

34181-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,7,7-hexachlorobicyclo[2.2.1]hept-2-en-5-ol

1.2 Other means of identification

Product number -
Other names (+-)-1,3-Diphenyl-hexan-1-on

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:34181-74-3 SDS

34181-74-3Relevant articles and documents

ENZYMATIC ACYLATION USING ACID ANHYDRIDES: CRUCIAL REMOVAL OF ACID

Berger, B.,Rabiller, C. G.,Koenigsberger, K.,Faber, K.,Griengl, H.

, p. 541 - 546 (2007/10/02)

An efficient enzymatic resolution of 7,7-disubstituted 1,4,5,6-tetrachlorobicyclohept-5-en-2-ols was accomplished by means of lipase AY-30 from Candida cylindracea in toluene.When acid anhydrides were used as acyl donors, the enantioselectivity was found to depend strongly on the reaction conditions: Whereas low selectivity (E 200).Alternatively, adsorption of the biocatalyst onto Celite was equally effective (E >300).Complete specificity was obtained when vinyl acetate was used as acyl donor (E ca.1000).

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