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59749-95-0

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59749-95-0 Usage

General Description

3-AMINO-N-CYCLOHEXYL-3-THIOXOPROPANAMIDE is an organic compound with a thioxopropionamide functional group and a cyclohexylamine substituent. It is commonly used as a building block in the synthesis of various pharmaceuticals and agricultural chemicals. This chemical has the potential to act as a chelating agent due to the presence of an amide and thio functional group, and it may also exhibit biological activity due to the amine group. Additionally, it has the potential to be a key intermediate in the production of other complex organic molecules. Its versatile reactivity and structural versatility make it a valuable component in organic synthesis, medicinal chemistry, and agricultural science.

Check Digit Verification of cas no

The CAS Registry Mumber 59749-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,4 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59749-95:
(7*5)+(6*9)+(5*7)+(4*4)+(3*9)+(2*9)+(1*5)=190
190 % 10 = 0
So 59749-95-0 is a valid CAS Registry Number.

59749-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-N-cyclohexyl-3-sulfanylidenepropanamide

1.2 Other means of identification

Product number -
Other names TOS-BB-0128

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:59749-95-0 SDS

59749-95-0Relevant articles and documents

E-Z-izomerization of 2-methylenethiazolidin-4-ones

Morzherin,Kosterina,Berseneva,Dehaen,Bakulev

, p. 1292 - 1297 (2007/10/03)

The equilibrium concentrations of E- and Z-isomers of thiazolidin-4-ones containing exocyclic double bonds in positions 2 and 5 of the cycle were determined in DMSO-d6. The influence of the nature of the substituents on the equilibrium position was found. Electron-releasing substituents stabilize the E,Z-configuration and electron-withdrawing substituents stabilize the Z,Z-configuration. The association constants of E- and Z-2-ethoxycarbonylmethylenethiazolidin-4-ones with the sodium cation were determined by 1H NMR spectroscopy.

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