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1H-Azepine-1-carbothioamide,hexahydro-N-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64575-42-4

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64575-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64575-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,7 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64575-42:
(7*6)+(6*4)+(5*5)+(4*7)+(3*5)+(2*4)+(1*2)=144
144 % 10 = 4
So 64575-42-4 is a valid CAS Registry Number.

64575-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Azepane-1-carbothioic acid methylamide

1.2 Other means of identification

Product number -
Other names -

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:64575-42-4 SDS

64575-42-4Downstream Products

64575-42-4Relevant academic research and scientific papers

Facile One-Pot Parallel Synthesis of 3-Amino-1,2,4-triazoles

Bogolyubsky, Andrey V.,Savych, Olena,Zhemera, Anton V.,Pipko, Sergey E.,Grishchenko, Alexander V.,Konovets, Anzhelika I.,Doroshchuk, Roman O.,Khomenko, Dmytro N.,Brovarets, Volodymyr S.,Moroz, Yurii S.,Vybornyi, Mykhailo

, p. 461 - 466 (2018)

A 1,2,4-triazole motif is present in numerous commercialized and investigational bioactive molecules. Despite its importance for medicinal chemistry, there is a lack of convenient combinatorial approaches toward this molecular core. Herein, we present a synthetic strategy suitable for the quick preparation of a library of structurally diverse 1,2,4-triazoles in a one-pot setting. The key steps include the formation of thioureas followed by S-alkylation using 1,3-propane sultone and consecutive ring closure leading to the desired 1,2,4-triazoles. Parallel synthesis yields thousands of 1,2,4-triazoles in a cost- and time-efficient manner from commercially available chemicals.

Nitroimidazoles: Part VII - 1-(1-Alkyl-5-nitroimidazol-2-yl)-aza(diaza,oxaza)cycloalkanes

Nagarajan, K.,Arya, V. P.,George, T.,Bhat, G.A.,Kulkarni, Y. S.,et al.

, p. 949 - 952 (2007/10/02)

Reaction of 1-methyl-2-methylsulphonyl-5-nitroimidazole (2) with pyrrolidine, piperidine and morpholine affords the amines (3a-c)(=9a-c) respectively in low yields, the reaction failing with other bases tried.Analogues (9d-t) have been obtained more readi

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