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49570-33-4

49570-33-4

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49570-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49570-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 49570-33:
(7*4)+(6*9)+(5*5)+(4*7)+(3*0)+(2*3)+(1*3)=144
144 % 10 = 4
So 49570-33-4 is a valid CAS Registry Number.

49570-33-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 3-methyl-1,2-thiazole-4,5-dicarboxylate

1.2 Other means of identification

Product number -
Other names 3-Methylisothiazol-4,5-dicarbonsaeuredimethylester

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:49570-33-4 SDS

49570-33-4Relevant articles and documents

ISOTHIAZOLE-PYRIDINE DERIVATIVES AS MODULATORS OF HIF (HYPOXIA INDUCIBLE FACTOR) ACTIVITY

-

Page/Page column 66, (2009/09/04)

The present invention relates to novel compounds according to Formula I or II, methods, and compositions capable of decreasing HIF hydroxylase enzyme activity, thereby increasing the stability and/or activity of hypoxia inducible factor (HIF). Formula (I) or (II).

THE THERMAL FRAGMENTATION OF 1,3,4-DITHIAZOL-2-ONES

Greig, Derek J.,Paton, R. Michael,Rankin, John G.,Ross, John F.,Crosby, John

, p. 5453 - 5454 (2007/10/02)

Thermal expulsion of carbon oxysulphide from 1,3,4-dithiazol-2-ones in the presence of DMAD affords nitrile sulphide-derived dimethyl isothiazole-4,5-dicarboxylates.

Some 1,3-Dipolar Cycloaddition Reactions of Nitrile N-Sulfides with Acetylenes and Olefins

Sanders, Michael J.,Grunwell, John R.

, p. 3753 - 3756 (2007/10/02)

The generation of nitrile N-sulfides from iminosulfur difluorides is general.Trifluoroacetonitrile N-sulfide was allowed to react with some acetylenes and olefins.For example, N-phenylmaleimide gave N-phenyl-3-trifluoromethyl-1,2-thiazoline-4,5-carboximid

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