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3020-73-3

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3020-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3020-73-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3020-73:
(6*3)+(5*0)+(4*2)+(3*0)+(2*7)+(1*3)=43
43 % 10 = 3
So 3020-73-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H11N.CHNS/c1-4(2,3)5;2-1-3/h5H2,1-3H3;3H

3020-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butylazanium,thiocyanate

1.2 Other means of identification

Product number -
Other names tert-Butylammoniumrhodanid

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:3020-73-3 SDS

3020-73-3Downstream Products

3020-73-3Relevant articles and documents

N,N-Disubstituted 2-Aminothiazole-5-carbaldehydes: Preparation and Investigation of Structural Features

Gillon, David W.,Forrest, Ian J.,Meakins, G. Denis,Tirel, Malcolm D.,Wallis, John D.

, p. 341 - 348 (2007/10/02)

Methods of preparing N,N-disubstituted 2-aminothiazoles have been investigated. 4-Substituted N,N-dimethyl-, N-benzyl-N-methyl-, and N-methyl-N-phenyl-amines were prepared and converted by Vilsmeier formylation into 2-amino-5-carbaldehydes which were examined by i.r. and 1H n.m.r. spectrometry.The aldehyde group adopts the carbonyl O,S-syn-conformation.With the N,N-dimethyl and N-benzyl-N-methyl compounds the barrier to rotation of the amine group (ΔG(excit.)) is 50-55 kJ mol-1 and is insensitive to the nature of the 4-substituent.The amine group of the N-methyl-N-phenyl compounds has a marked preference for one orientation.This was shown by a crystallographic study of 4-t-butyl-2-(N-methyl-N-phenylamino)thiazole-5-carbaldehyde to have the phenyl group directed towards the sulphur atom of the thiazole ring.

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