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TCI

CAS 138564-58-6

2-Amino-5-methyl-3-thiophenecarbonitrile TCI A2351

2-Amino-5-methyl-3-thiophenecarbonitrile TCI A2351

Chemical Identity

CAS No.
138564-58-6
PubChem
CID 689056·SID 135727254
Formula
C6H6N2S
Molecular weight
138.19 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-amino-5-methylthiophene-3-carbonitrile
SMILES
CC1=CC(=C(S1)N)C#N
InChIKey
YGXADLPRHBRTPG-UHFFFAOYSA-N
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2-Amino-5-methyl-3-thiophenecarbonitrile is a chemical compound classified under the category of heterocyclic building blocks. It plays a crucial role in laboratory settings, particularly in the synthesis of complex molecules with heterocyclic structures. This compound is widely used in organic chemistry research and industrial chemical applications due to its structural versatility and reactivity. Its unique molecular framework allows it to participate in various chemical reactions, making it an essential reagent for chemists working on the development of new compounds.

The compound's chemical properties make it a preferred choice for synthetic chemists. It exhibits stability under controlled conditions but is sensitive to oxidation and uncontrolled chemical reactions. This sensitivity requires careful handling during storage and use. The heterocyclic structure of the molecule contributes to its reactivity, enabling it to be used in substitution and condensation reactions. Its chemical stability and reactivity make it a valuable tool in the synthesis of pharmaceuticals and other complex organic compounds.

In Indonesian laboratories, 2-Amino-5-methyl-3-thiophenecarbonitrile is commonly used in organic chemistry research. It is a key reagent in the synthesis of new compounds and is widely utilized by research institutions and universities. Its application is particularly prominent in projects focused on the development of novel pharmaceuticals and industrial chemicals. The compound's versatility and reactivity make it an essential component in many experimental setups across the country.

TCI brochures (PDF)

  • Organic synthesis of heterocyclic compounds due to its reactive thiophene core and amino group.
  • Development of pharmaceuticals and industrial chemicals through structural modification and functional group introduction.
  • Research in medicinal chemistry for the design of new drug molecules with targeted biological activity.
  • Preparation of complex organic intermediates for further chemical transformations and derivatization.
  • Investigation of reaction mechanisms involving heterocyclic ring systems and nucleophilic substitution processes.

Brand TCI
CAS number 138564-58-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes As per supplier specification
Physical form Solid (as per supplier specification)
Storage Store in a cool, dry place away from light and incompatible materials.

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which may lead to oxidation. Due to its sensitivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances like strong oxidizing agents. Ensure proper ventilation in the workspace to minimize inhalation risks. Always follow standard laboratory safety protocols when working with this material.

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