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1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120405-13-2 Structure
  • Basic information

    1. Product Name: 1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI)
    2. Synonyms: 1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI)
    3. CAS NO:120405-13-2
    4. Molecular Formula: C3H3N3OS2
    5. Molecular Weight: 161.20542
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 120405-13-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI)(120405-13-2)
    11. EPA Substance Registry System: 1,2,3-Thiadiazole-4-carboxamide,5-mercapto-(9CI)(120405-13-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 120405-13-2(Hazardous Substances Data)

120405-13-2 Usage

Thiadiazole family

Member
The compound belongs to the thiadiazole family, which is a group of five-membered heterocyclic compounds containing sulfur and nitrogen atoms.

Carboxamide group

Present
The compound contains a carboxamide group (-CONH2), which is an amide derived from carboxylic acid.

Mercapto group

Present
The compound also contains a mercapto group (-SH), which is a functional group consisting of a sulfur atom bonded to a hydrogen atom.

Potential applications

Pharmaceuticals and agrochemicals
Due to its versatile properties, the compound may be used in the development of pharmaceuticals and agrochemicals.

Biological activities

Antimicrobial, antiviral, and antifungal properties
The compound may exhibit biological activities such as antimicrobial, antiviral, and antifungal properties, making it a potential candidate for further research in these areas.

Building block

Organic synthesis
The compound can be used as a building block in organic synthesis for the development of new compounds with diverse functions and applications.

Chemical structure

Interesting target for research and development
The unique chemical structure of the compound makes it an interesting target for further research and development in various fields of science and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 120405-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,0 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120405-13:
(8*1)+(7*2)+(6*0)+(5*4)+(4*0)+(3*5)+(2*1)+(1*3)=62
62 % 10 = 2
So 120405-13-2 is a valid CAS Registry Number.

120405-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-sulfanylidene-2H-thiadiazole-4-carboxamide

1.2 Other means of identification

Product number -
Other names 1,2,3-thiadiazole-4-carboxamide,5-mercapto

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:120405-13-2 SDS

120405-13-2Downstream Products

120405-13-2Relevant articles and documents

NUCLEOPHILIC SUBSTITUTION IN 1,2,3-THIADIAZOLES

Morzherin, Yu. Yu.,Tarasov, E. V.,Bakulev, V. A.

, p. 489 - 494 (2007/10/02)

By reactions of nucleophilic substitution of the halogen atom in 5-halo-1,2,3-thiadiazoles (IV), we have obtained 5-amino- (I, V), hydrazino- (VI, VII, IX, X), and mercapto- (VIII) 1,2,3-thiadiazoles.We show that upon reaction with amines, a mixture of 5-

Cephalosporin compounds and antibacterial agents

-

, (2008/06/13)

Cephalosporin compounds of the formula (I): STR1 wherein R1 and R2 may be the same or different and are a hydrogen atom or a lower alkyl group of 1-5 carbon atoms and A is a hydrogen atom or a nucleophilic compound residue or pharmacologically acceptable salts thereof have excellent antibacterial activity against Gram positive and Gram negative microorganisms.

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