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59130-21-1

59130-21-1

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59130-21-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59130-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59130-21:
(7*5)+(6*9)+(5*1)+(4*3)+(3*0)+(2*2)+(1*1)=111
111 % 10 = 1
So 59130-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12Cl2/c16-15(17)13(11-7-3-1-4-8-11)14(15)12-9-5-2-6-10-12/h1-10,13-14H

59130-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dichloro-trans-2,3-diphenylcyclopropane

1.2 Other means of identification

Product number -
Other names E-1,1-dichloro-2,3-diphenylcyclopropane

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:59130-21-1 SDS

59130-21-1Relevant articles and documents

New multi-site phase transfer catalyst for the addition of dichlorocarbene to olefins

Shanmugan,Balakrishnan

, p. 1069 - 1074 (2008/02/11)

Three step synthesis of a new, water-soluble multi-site phase transfer catalyst (MPTC-I), viz., α,α1,α11- tris(triethyl ammonium methylene bromide) β-hydroxy ethyl benzene is described. The potentiality of MPTC-I is demonstrated by studying kinetic aspects of the reactions, viz. dichlorocarbene addition to styrene, α-methyl styrene and trans-stilbene.

THERMAL TRANSFORMATIONS OF GEM-DIHALOGENODIPHENYLCYCLOPROPANES

Kostikov, R. R.,Varakin, G. S.,Ogloblin, K. A.

, p. 1438 - 1444 (2007/10/02)

When gem-dihalogenodiphenylcyclopropanes are heated, 2-halogenophenylindenes or diphenyl-2-halogeno-1,3-alkadienes are formed.The yields of the substituted indenes are increased in the presence of acidic catalysts, while the yield of the dienes is increas

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