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182479-74-9

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182479-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182479-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 182479-74:
(8*1)+(7*8)+(6*2)+(5*4)+(4*7)+(3*9)+(2*7)+(1*4)=169
169 % 10 = 9
So 182479-74-9 is a valid CAS Registry Number.

182479-74-9SDS

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 5-(Bromomethyl)-6-chloro-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 5-(bromomethyl)-6-chlorobenzo[d][1,3]dioxole

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:182479-74-9 SDS

182479-74-9Downstream Products

182479-74-9Relevant articles and documents

PYRROLIDINEANILINES

-

Page/Page column 124, (2010/11/27)

The present invention relates to a compotind represented by the following formula I or a pharmaceutically acceptable salt thereof; wherein R1, R2, and y are defined herein. The present invention further relates to compositions that include the compound of the present invention as well as a method of treating a patient from endometreosis or uterine fibroids.

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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