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134619-72-0

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134619-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134619-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,1 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 134619-72:
(8*1)+(7*3)+(6*4)+(5*6)+(4*1)+(3*9)+(2*7)+(1*2)=130
130 % 10 = 0
So 134619-72-0 is a valid CAS Registry Number.

134619-72-0SDS

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 4-(4-chlorophenyl)-4-bromo-1-butene

1.2 Other means of identification

Product number -
Other names -

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:134619-72-0 SDS

134619-72-0Relevant articles and documents

Boron trihalide mediated haloallylation of aryl aldehydes and its application to the preparation of (E)-1,3-dienes

Quinn, Michael P.,Yao, Min-Liang,Yong, Li,Kabalka, George W.

experimental part, p. 3815 - 3820 (2012/01/05)

In the presence of boron trihalides, aryl aldehydes couple readily with allylmetals to afford haloallylated products. The reactions tolerate a variety of functional groups. Simple aqueous workup of haloallylation reactions, followed by treatment with 1,8-

Efficient and selective halogenation of allylic and benzylic alcohols under mild conditions

Bandgar, Babasaheb P.,Bettigeri, Sampada V.

, p. 1251 - 1255 (2007/10/03)

A simple, mild, and high yielding procedure for the halogenation of allylic and benzylic alcohols using a combination of SOCl2, benzotriazole, and potassium halides in DMF is described. The effectiveness of the protocol is manifested in its selectivity towards allylic and benzylic alcohols whereas other simple alcohols such as primary, secondary, and tertiary are found to be unreactive. Springer-Verlag 2004.

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