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4-Ethyloxazolidine-2-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13997-20-1

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13997-20-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13997-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,9 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13997-20:
(7*1)+(6*3)+(5*9)+(4*9)+(3*7)+(2*2)+(1*0)=131
131 % 10 = 1
So 13997-20-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NOS/c1-2-4-3-7-5(8)6-4/h4H,2-3H2,1H3,(H,6,8)

13997-20-1SDS

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 4-Ethyl-2-oxazolidinethione

1.2 Other means of identification

Product number -
Other names 4-Aethyl-oxazolidin-2-thion

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:13997-20-1 SDS

13997-20-1Downstream Products

13997-20-1Relevant academic research and scientific papers

Synthesis of cyclic N-nitrourethanes by the simultaneous oxidative desulfurization and nitration of cyclic thiourethanes

Willer, Rodney L.,Campbell, Christopher G.,Storey, Robson F.

experimental part, p. 421 - 423 (2012/06/18)

The reaction of five- and six-membered cyclic thiourethanes with acetyl nitrate results in a vigorous reaction that generates copious amounts of red-brown nitrogen oxide fumes and produces the corresponding cyclic N-nitrourethanes in high yields (>95%). The overall yield of the cyclic N-nitrourethanes starting from an aminoalcohol using the " thiourethane" route is superior to the conventional route going through the cyclic urethane. Copyright

A convenient method for the synthesis of substituted thioureas

Maddani, Mahagundappa,Prabhu, Kandikere Ramaiah

, p. 7151 - 7154 (2008/03/11)

A convenient method for the synthesis of substituted thioureas by the reaction of primary amines with molybdenum dialkyl dithiocarbamates has been developed. Primary amines on reaction with 0.5 equiv of molybdenum xanthate produce the corresponding thiour

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