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Carbamimidothioic acid, N-cyano-N'-ethyl-, methyl ester, also known as methyl N-cyano-N'-ethylcarbamimidothioate, is a chemical compound with the molecular formula C6H10N2S. It is a derivative of carbamimidothioic acid, featuring a cyano group (-CN), an ethyl group (-C2H5), and a methyl ester group (-OCH3) attached to the nitrogen atoms. Carbamimidothioic acid, N-cyano-N'-ethyl-, methyl ester is primarily used as an intermediate in the synthesis of various agrochemicals, pharmaceuticals, and other organic compounds. Its chemical structure and reactivity make it a valuable building block in the development of new molecules with potential applications in various industries.

5848-25-9

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5848-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5848-25-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5848-25:
(6*5)+(5*8)+(4*4)+(3*8)+(2*2)+(1*5)=119
119 % 10 = 9
So 5848-25-9 is a valid CAS Registry Number.

5848-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N-cyano-N'-ethylcarbamimidothioate

1.2 Other means of identification

Product number -
Other names N-Aethyl-N'-cyan-S-methyl-isothioharnstoff

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:5848-25-9 SDS

5848-25-9Relevant academic research and scientific papers

On triazoles XLV [1]. Synthesis of 5,7-diamino-1,2,4-triazolo[1,5-a][1,3,5]triazines

Berecz, Gabor,Pongo, Laszlo,Koevesdi, Istvan,Reiter, Jozsef

, p. 327 - 334 (2007/10/03)

The reaction of differently substituted 5-amino-1,2,4-triazoles (5) with isothiourea derivatives (3) to yield isomeric 5,7-diamino-1,2,4-triazolo[1,5-a][1,3,5]triazines (6 and 7), previously described as not proceeding in melt, was performed in different solvents as well as in the melt at 150-160°. It was proved that the above reaction had rather general validity. The structure of isomers 6 and 7 were proved spectroscopically. The structure of 6/5 (Q = ethylamino) was corroborated with single crystal X-ray diffraction determination, as well.

First synthesis of 4-substituted benzenesulfonylcyanoguanidines

Masereel, Bernard,Lebrun, Philippe,Dogne, Jean Michel,De Tullio, Pascal,Pirotte, Bernard,Pochet, Lionel,Diouf, Ousman,Delarge, Jacques

, p. 7253 - 7254 (2007/10/03)

N'-substituted-N-cyano-S-methylcarbamimidothioates react with 4-substituted benzene sulfonamides to give the corresponding sulfonylcyanoguanidines.

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