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180847-73-8

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180847-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180847-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,8,4 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 180847-73:
(8*1)+(7*8)+(6*0)+(5*8)+(4*4)+(3*7)+(2*7)+(1*3)=158
158 % 10 = 8
So 180847-73-8 is a valid CAS Registry Number.

180847-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-Dichloro-1,3-diphenylpropane

1.2 Other means of identification

Product number -
Other names 1,3-dichloro-1,3-diphenylpropane

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:180847-73-8 SDS

180847-73-8Relevant articles and documents

Lewis acid mediated reactions of aldehydes with styrene derivatives: Synthesis of 1,3-Dihalo-1,3-diarylpropanes and 3-chloro-1,3-diarylpropanols

Kabalka, George W.,Wu, Zhongzhi,Ju, Yuhong,Yao, Min-Liang

, p. 10285 - 10291 (2007/10/03)

The reactions of aryl aldehydes with styrene derivatives, mediated by various boron Lewis acids, were investigated. 1,3-Dihalo-1,3-diarylpropanes were obtained in high yields with boron trihalides, while 3-chloro-1,3- diarylpropanols were obtained in good

Synthesis of 4,5-dihydroisoxazoles from arylcyclopropanes and nitrosyl chloride

Bondarenko,Gavrilova,Saginova,Zyk

, p. 1021 - 1024 (2007/10/03)

Arylcyclopropanes readily react with nitrosyl chloride in liquid sulfur dioxide to give the corresponding 5-aryl-4,5-dihydroisoxazoles in good yield. The reaction is most selective at -40 to -50°C; at higher temperature, the contribution of side processes

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