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1030632-94-0

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1030632-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1030632-94-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,0,6,3 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1030632-94:
(9*1)+(8*0)+(7*3)+(6*0)+(5*6)+(4*3)+(3*2)+(2*9)+(1*4)=100
100 % 10 = 0
So 1030632-94-0 is a valid CAS Registry Number.

1030632-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Ethyl-2-(trifluoromethyl)pyridine

1.2 Other means of identification

Product number -
Other names 3-ethyl-6-trifluoromethyl pyridine

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:1030632-94-0 SDS

1030632-94-0Downstream Products

1030632-94-0Relevant articles and documents

METHODS FOR PREPARING 3-SUBSTITUTED-6-TRIFLUOROMETHYL PYRIDINES AND METHODS FOR USING 6-TRICHLOROMETHYL HALOGENATED PYRIDINES

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, (2013/10/08)

3-substituted-6-trifluoromethyl pyridines are useful synthetic intermediates in the preparation of the N-substituted (6-haloalkylpyridin-3-yl)alkyl sulfoximines, which are useful in forming potent insecticides. Methods of forming such 3-substituted-6-trifluoromethyl pyridines are disclosed. Also disclosed are methods of using 6-trichloromethyl halogenated pyridines to form 3-substituted-6-trifluoromethyl pyridines are disclosed.

Process for the preparation of 2-substituted-5-(1-alkylthio)alkylpyridines

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Page/Page column 4, (2008/12/05)

2-Substituted-5-(1-alkylthio)alkylpyridines are produced efficiently and in high yield by cyclization and thioalkylation.

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