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20057-31-2

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  • TavronCAS NO.20057-31-2 CAS NO.20057-31-2 CAS NO.20057-31-2

    Cas No: 20057-31-2

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20057-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20057-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,5 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20057-31:
(7*2)+(6*0)+(5*0)+(4*5)+(3*7)+(2*3)+(1*1)=62
62 % 10 = 2
So 20057-31-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9Cl3/c1-8(7-10(11,12)13)9-5-3-2-4-6-9/h2-6H,1,7H2

20057-31-2SDS

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 tavron

1.2 Other means of identification

Product number -
Other names Benzene,(3,3,3-trichloro-1-methylenepropyl)

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:20057-31-2 SDS

20057-31-2Relevant articles and documents

A half-sandwich 1,2-azaborolyl ruthenium complex: Synthesis, characterization, and evaluation of its catalytic activities

Liu, Zicheng,Xu, Junjie,Ruan, Wenqing,Fu, Chen,Zhang, Hui-Jun,Wen, Ting-Bin

supporting information, p. 11976 - 11980 (2013/09/02)

A half-sandwich 1,2-azaborolyl (Ab) ruthenium complex, (Ab-CCPh) RuCl(PPh3)2 (1), has been synthesized by treating RuCl2(PPh3)3 with lithium 1,2-azaborolide L-1, or by treating either RuCl2(PPh3)3 or RuHCl(PPh3)3 directly with 1,2-azaborole LH-1. It is evaluated as a suitable precatalyst in [2 + 2] cycloadditions of norbornene derivatives with DMAD and in atom transfer radical additions of halogenated compounds with olefins. The Royal Society of Chemistry.

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