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80673-02-5

80673-02-5

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80673-02-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80673-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,7 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80673-02:
(7*8)+(6*0)+(5*6)+(4*7)+(3*3)+(2*0)+(1*2)=125
125 % 10 = 5
So 80673-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl3NO/c8-7(9,10)6(12)5-3-1-2-4-11-5/h1-4,6,12H

80673-02-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trichloro-1-pyridin-2-ylethanol

1.2 Other means of identification

Product number -
Other names 2-Pyridyltrichloromethyl carbinol

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:80673-02-5 SDS

80673-02-5Relevant articles and documents

Decarboxylative trichloromethylation of aromatic aldehydes and its applications in continuous flow

Jensen, Andreas B.,Lindhardt, Anders T.

, p. 1174 - 1183 (2014/03/21)

Two new protocols for the efficient synthesis of 2,2,2- trichloromethylcarbinols, starting from aromatic aldehydes, have been developed. A combination of sodium trichloroacetate in the presence of malonic acid proved efficient for the transformation of el

Copper(I)-promoted synthesis of chloromethyl ketones from trichloromethyl carbinols

Ram, Ram N.,Manoj

, p. 5633 - 5635 (2008/12/21)

(Chemical Equation Presented) Reaction of several trichloromethyl carbinols with 2 equiv of CuCl/bpy in refluxing DCE for 3 h afforded chloromethyl ketones in excellent yield by 1,2-H shift in the copper-chlorocarbenoid intermediate.

New syntheses of trichloromethyl functional alcohols. Studies of tranquilizing properties

Deleris,Dunogues,Babin,et al.

, p. 533 - 537 (2007/10/02)

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