3-Methylthiophene-2-carboxaldehyde - ≥85%(GC) , CAS No.5834-16-2

CAS: 5834-16-2 Cat. No.: M157936 Molecular Weight: 126.17 Beilstein Registry Number: 107874 EC Number: 227-418-8

GRADE & PURITY ≥85%(GC)

Synonyms

3-Methyl-2-thiophenecarboxaldehyde, tech grade | thiophene, 3-Methyl, 2-formyl | UNII-ZHC9WE8PS0 | AM20100422 | SCHEMBL447131 | 3-methyl-thiophene-2-carbaldehyde | 3-Methylthiophene-2-carbaldehyde | MORANTEL HYDROGEN TARTRATE IMPURITY E [EP IMPURITY] | 3-

Storage

Argon charged,Room temperature

Shipped In

Normal

Overview

3-Methylthiophene-2-carboxaldehyde was used in the synthesis of 2,3-dimethyl-5-(2,6,10-trimethylundecyl)thiophene. It was used to investigate versatile bioconversion capacity of baker′s yeast for the generation of thiols from cysteine-aldehyde conjugates.

Specifications

Synonyms

3-Methyl-2-thiophenecarboxaldehyde, tech grade | thiophene, 3-Methyl, 2-formyl | UNII-ZHC9WE8PS0 | AM20100422 | SCHEMBL447131 | 3-methyl-thiophene-2-carbaldehyde | 3-Methylthiophene-2-carbaldehyde | MORANTEL HYDROGEN TARTRATE IMPURITY E [EP IMPURITY] | 3-

Specifications & Purity

≥85%(GC)

Storage

Argon charged, Room temperature

Shipped In

Normal

Purity

≥85%(GC)

Names and Identifiers

• Pubchem Sid: 488185800
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488185800
• Canonical Smiles: CC1=C(SC=C1)C=O
• IUPAC Name: 3-methylthiophene-2-carbaldehyde
• InChIKey: BSQKBHXYEKVKMN-UHFFFAOYSA-N
• INCHI: 1S/C6H6OS/c1-5-2-3-8-6(5)4-7/h2-4H,1H3
• Isomeric SMILES: CC1=C(SC=C1)C=O
• WGK Germany: 3
• Molecular Weight: 126.17
• Beilstein: 107874
• Reaxy-Rn: 107874
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107874&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Aldehydes
          • Level6 Aryl-aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Aldehydes
• Direct Parent: Aryl-aldehydes
• Alternative Parents: Thiophenes Heteroaromatic compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Aryl-aldehyde - Heteroaromatic compound - Thiophene - Organoheterocyclic compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aryl-aldehydes. These are compounds containing an aldehyde group directly attached to an aromatic ring.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: Insoluble in water
• Sensitivity: Air sensitive
• Refractive Index: 1.5870
• Flash Point(°F): 179.6 °F
• Flash Point(°C): 82 °C
• Boil Point(°C): 215°
• Molecular Weight: 126.180 g/mol
• XLogP3: 1.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 126.014 Da
• Monoisotopic Mass: 126.014 Da
• Topological Polar Surface Area: 45.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 92.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1