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Carbamic acid, sulfinyl-, ethyl ester, also known as ethyl N-hydroxycarbamate sulfinate, is an organic compound with the chemical formula C3H7NO3S. It is a colorless liquid that is soluble in water and has a molecular weight of 135.16 g/mol. Carbamic acid, sulfinyl-, ethyl ester is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other chemical products. It is also known for its potential applications in the development of new materials and as a reagent in various chemical reactions. Due to its reactivity, it is essential to handle Carbamic acid, sulfinyl-, ethyl ester with care, following proper safety protocols to minimize any potential hazards.

5659-92-7

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5659-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5659-92-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5659-92:
(6*5)+(5*6)+(4*5)+(3*9)+(2*9)+(1*2)=127
127 % 10 = 7
So 5659-92-7 is a valid CAS Registry Number.

5659-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-sulfinylcarbamate

1.2 Other means of identification

Product number -
Other names WWKLPECCKCCXBJ-UHFFFAOYSA

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:5659-92-7 SDS

5659-92-7Upstream product

5659-92-7Relevant academic research and scientific papers

Reactions of N-Sulfinyl Compounds, XV. - Synthesis of 2-Alkenesulfinic Acid Amides - Structure-Reactivity Relationships for N-Sulfinyl Compounds as Enophiles

Bussas, Reinhard,Kresze, Guenter

, p. 545 - 563 (2007/10/02)

The reactivity of N-sulfinyl compounds R6NSO 2 in ene-reactions shows a large variation depending on the nature of the group R6.Haloalkanesulfonamide derivatives react even with very unreactive alkenes.The scope of this method for the synthesis of sulfinic acid amides and the side reactions are discussed.

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