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37729-56-9

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37729-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37729-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,2 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 37729-56:
(7*3)+(6*7)+(5*7)+(4*2)+(3*9)+(2*5)+(1*6)=149
149 % 10 = 9
So 37729-56-9 is a valid CAS Registry Number.

37729-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-chloroethyl)-4-phenylbenzene

1.2 Other means of identification

Product number -
Other names 1-(4-biphenylyl)-2-chloroethane

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:37729-56-9 SDS

37729-56-9Relevant articles and documents

Selective activation of 1,2-dichloroethane for access to β-chloroethylarenes enabled by nickel-catalyzed suzuki-type couplings

Yang, Yi,Cai, Junjie,Luo, Gen,Tong, Xia,Su, Yumei,Jiang, Yan,Liu, Yingle,Zheng, Yubin,Zeng, Jijiao,Li, Chaolin

, p. 1130 - 1134 (2019)

The selective conversion of one inactive C(sp3)-Cl bond of 1,2-dichloroethane (DCE) into C(sp3)-C(sp2) linkages for access to β-chloroethylarenes is presented here. The key to achieve the required reactivity and chemoselectivity in this synthetic method was the utilization of nickel and combinatorial nitrogen ligands as catalytic system. Synthetic advantages of this coupling chemistry included the step-simplicities to β-chloroethylarenes, the mildness and effectiveness of coupling conditions, together with the convenience for allowing further functional group transformations of the retained homobenzylic C–Cl bonds.

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