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Catalog Number:
44311
CAS Number:
72835-25-7
5-Methylthiophene-2-carbonitrile
Purity:
≥ 98% (GC)
Synonym(s):
2-Cyano-5-methylthiophene
Hazmat
Documents
$143.01 /1G
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Product Information
Synonyms
2-Cyano-5-methylthiophene
CAS Number
72835-25-7
Purity
≥ 98% (GC)
Molecular Formula
C6H5NS
Molecular Weight
0
MDL Number
MFCD01434334
PubChem ID
312733
Density
1.12
Appearance
Colorless to light yellow to light orange clear liquid
Boiling Point
90 °C/10 mmHg
Refractive Index
n20D 1.56
Conditions
Store at RT
General Information
Synonyms
2-Cyano-5-methylthiophene
CAS Number
72835-25-7
Purity
≥ 98% (GC)
Molecular Formula
C6H5NS
Molecular Weight
0
MDL Number
MFCD01434334
PubChem ID
312733
Density
1.12
Appearance
Colorless to light yellow to light orange clear liquid
Boiling Point
90 °C/10 mmHg
Refractive Index
n20D 1.56
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Methylthiophene-2-carbonitrile is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important building block in the synthesis of various pharmaceuticals, particularly in developing drugs that target neurological disorders.
  • Agrochemical Formulations: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides, which helps in improving crop yields and protecting plants from pests.
  • Material Science: The compound is explored in the development of advanced materials, including conductive polymers, which are essential in electronics and energy storage applications.
  • Flavor and Fragrance Industry: Its unique aroma profile makes it valuable in creating flavoring agents and fragrances, providing a distinct scent in various consumer products.
  • Research in Organic Synthesis: 5-Methylthiophene-2-carbonitrile is a key intermediate in organic synthesis, facilitating the creation of complex molecules in laboratory settings, thus aiding researchers in exploring new chemical pathways.

Citations