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5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide, a member of the thiophene family, is a chemical compound with the molecular formula C13H9N3OS. It is characterized by a five-membered ring containing four carbon atoms and one sulfur atom, and is classified as an amide due to the presence of a carbonyl group and an amino group attached to the carbon atom. This yellow crystalline solid is utilized in the synthesis of pharmaceuticals and organic compounds, making it a valuable component in the development of novel drugs and organic materials in the field of chemistry and pharmaceutical research.

70541-99-0

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70541-99-0 Usage

Uses

Used in Pharmaceutical Synthesis:
5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide is used as an intermediate in the synthesis of various pharmaceuticals for its unique molecular structure and properties. It contributes to the development of novel drugs with potential therapeutic applications.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide serves as a key component in the synthesis of organic compounds. Its distinctive structure allows for the creation of new organic materials with specific properties and potential applications in various industries.
Used in Chemical Research:
5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide is utilized in chemical research to explore its properties and potential reactions with other compounds. This research aids in understanding its behavior and reactivity, which can lead to the discovery of new chemical processes and applications.
Used in Drug Development:
In the pharmaceutical industry, 5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide is used as a building block in drug development. Its unique structure and properties make it a promising candidate for the creation of new drugs with improved efficacy and selectivity.
Used in Material Science:
5-Cyano-4-methyl-3-phenyl-2-thiophenecarboxamide is employed in material science for the development of new organic materials. Its molecular structure allows for the design of materials with specific properties, such as conductivity, stability, or reactivity, which can be applied in various technological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 70541-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70541-99:
(7*7)+(6*0)+(5*5)+(4*4)+(3*1)+(2*9)+(1*9)=120
120 % 10 = 0
So 70541-99-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2OS/c1-8-10(7-14)17-12(13(15)16)11(8)9-5-3-2-4-6-9/h2-6H,1H3,(H2,15,16)

70541-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-cyano-4-methyl-3-phenylthiophene-2-carboxamide

1.2 Other means of identification

Product number -
Other names cyanomethylphenylthiophenecarboxamide

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:70541-99-0 SDS

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