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6326-86-9

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6326-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6326-86-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6326-86:
(6*6)+(5*3)+(4*2)+(3*6)+(2*8)+(1*6)=99
99 % 10 = 9
So 6326-86-9 is a valid CAS Registry Number.

6326-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2,5,5-trimethyl-4H-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names 2,5,5-Trimethyl-4,5-dihydro-thiazol-4-carbonsaeure-methylester

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:6326-86-9 SDS

6326-86-9Downstream Products

6326-86-9Relevant articles and documents

Synthesis and Nuclear Magnetic Resonance Study of 2-Thiazolines

Eggleton, Gordon L.,Bushman, Daniel R.,Whitlock, David W.,Pugh, Darrell K.,Chance, Katherine L.

, p. 351 - 354 (2007/10/02)

A series of 5,5-dimethyl-2-thiazoline-4-carboxylates with a phenyl or methyl group at the 2-position of the ring were prepared from the corresponding methyl or ethyl ester of penicillamine and either methyl benzimidate or ethyl acetimidate.The free acid was obtained by the reaction of penicillamine with benzonitrile to produce 5,5-dimethyl-2-phenyl-2-thiazoline-4-carboxylic acid.Corresponding thiazolines were prepared from cysteine in the same manner.The nuclear magnetic resonance spectra of both series exhibit coupling of the methyl group at the 2-position with the hydrogen at the 4-position.The groups at the 5-position are nonequivalent and in the case of the cysteine series give rise to an ABX system.Further analysis confirms a concentration dependence for this splitting pattern.

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