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116252-52-9

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116252-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116252-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,2,5 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116252-52:
(8*1)+(7*1)+(6*6)+(5*2)+(4*5)+(3*2)+(2*5)+(1*2)=99
99 % 10 = 9
So 116252-52-9 is a valid CAS Registry Number.

116252-52-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-1-(1,3-thiazol-4-yl)methanamine

1.2 Other means of identification

Product number -
Other names 4-thiazolemethanamine,n,n-dimethyl

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:116252-52-9 SDS

116252-52-9Downstream Products

116252-52-9Relevant articles and documents

NOVEL COMPOUNDS

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Paragraph 0266; 0267; 0268, (2015/06/24)

Heterocyclic compounds and salts according to formula (I), which are pyrimidinone derivatives, described herein exhibit human neutrophil elastase inhibitory properties, and useful for treating diseases or conditions in which HNE is implicated.

Carbene structure of stable acyl (formyl) anion equivalents

Hilf, Christof,Bosold, Ferdinand,Harms, Klaus,Lohrenz, John C. W.,Marsch, Michael,Schimeczek, Michael,Boche, Gernot

, p. 1201 - 1212 (2007/10/03)

3-Lithiated 4-terNbutyl-imidazol-2-ylidene, 3-lithiated 4-tert butyl-thiazol-2-ylidene, and the ZnBr species of the latter, are shown to be stable carbenes by X-ray crystal structure determination. The crystal data are confirmed by 13C-NMR investigations in solution and quantum-chemical calcula tions. The exceptional stability of these acyl anion equiva-lents is due to the p(n) stabilization of the carbene carbon atoms by the adjacent amino (thio) substituents, as is also the case in the structurally related stable carbenes, which have recently been isolated for the first time by A. J. Arduengo III et al., and in stable nitrenium ions, as found by our group. VCH Verlagsgesellschaft mbH.

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