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85059-20-7

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85059-20-7 Usage

Structure

Thiadiazole derivative
It is a heterocyclic compound with a five-membered ring containing two nitrogen and one sulfur atom.

Contains an amide group

-CONH2
The presence of an amide group contributes to the compound's reactivity and potential applications.

Contains an amino group

-NH2
The amino group is another functional group that can participate in various chemical reactions and interactions.

Potential applications

Biochemical and pharmaceutical
Due to its unique structure and functional groups, this compound may have uses in the development of new drugs and therapies.

Promising candidate for research

Drug discovery and development
Its chemical properties and structure make it a valuable subject for further investigation in the field of medicinal chemistry.

Fields of interest

Antimicrobial and antiparasitic agents
The compound's properties suggest that it may be effective against various microorganisms and parasites, making it a candidate for the development of new treatments in these areas.

Pharmacological importance

Potential therapeutic applications
The compound's unique structure and properties indicate that it may have significant therapeutic potential, warranting further study and research.

Check Digit Verification of cas no

The CAS Registry Mumber 85059-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85059-20:
(7*8)+(6*5)+(5*0)+(4*5)+(3*9)+(2*2)+(1*0)=137
137 % 10 = 7
So 85059-20-7 is a valid CAS Registry Number.

85059-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminothiadiazole-4-carboxamide

1.2 Other means of identification

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

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:85059-20-7 SDS

85059-20-7Upstream product

85059-20-7Relevant articles and documents

DUAL REACTIVITY OF 2-DIAZO-2-CYANOACETAMIDE RELATIVE TO HYDROGEN SULFIDE

Bakulev, V. A.,Kolobov, M. Yu.,Grishakov, A. N.,Mokrushin, V. S.

, p. 178 - 180 (2007/10/02)

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HETEROCYCLIZATION OF COMPOUNDS CONTAINING DIAZO AND CYANO GROUPS. 2. SYNTHESIS AND RECYCLIZATION OF 4-SUBSTITUTED 5-AMINO-1,2,3-THIADIAZOLES

Shafran, Yu. M.,Bakulev, B. A.,,Mokrushin, V. S.,Validuda, G. I.

, p. 567 - 571 (2007/10/02)

The reaction of carbonyl derivatives of diazoacetonitrile with hydrogen sulfide in the presence of triethylamine yields 4-substituted 5-amino-1,2,3-thiadiazoles.Under analogous conditions, hydrogen selenide and ethyl mercaptan reduce the starting diazo co

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