Cas no 219834-79-4 (2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine)

2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine structure
219834-79-4 structure
Product Name:2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine
CAS No:219834-79-4
MF:C8H10N2
MW:134.178401470184
CID:243728
PubChem ID:11018918
Update Time:2025-09-23

2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine Chemical and Physical Properties

Names and Identifiers

    • 2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine
    • 1H-Pyrrolo[3,2-c]pyridine,2,3-dihydro-1-methyl-
    • 1-Methyl-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine
    • 1-Methyl-2,3-dihydro-1H-indole-5-carboxylic acid
    • 1-methyl-2,3-dihydro-1H-pyrrolo< 3,2-c> pyridine
    • 1-methyl-2-pyrrolino[3,2-c]pyridine
    • 1-Methylindoline-5-carboxylic acid
    • 5-Carboxy-1-methylindoline
    • AM803818
    • CC58701
    • N-methylindoline-5-carboxylic acid
    • SBB089265
    • SureCN2819895
    • 1-methyl-1H,2H,3H-pyrrolo[3,2-c]pyridine
    • SCHEMBL256358
    • 219834-79-4
    • EN300-412381
    • 1H-Pyrrolo[3,2-c]pyridine,2,3-dihydro-1-methyl-(9CI)
    • 1-methyl-2,3-dihydropyrrolo[3,2-c]pyridine
    • Inchi: 1S/C8H10N2/c1-10-5-3-7-6-9-4-2-8(7)10/h2,4,6H,3,5H2,1H3
    • InChI Key: XSDNNOKMBGISOS-UHFFFAOYSA-N
    • SMILES: N1(C)C2C=CN=CC=2CC1

Computed Properties

  • Exact Mass: 134.084398327g/mol
  • Monoisotopic Mass: 134.084398327g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 124
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1
  • Topological Polar Surface Area: 16.1?2

2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine Pricemore >>

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2,3-dihydro-1-methyl-1H-Pyrrolo[3,2-c]pyridine Related Literature

  • 1. Atropisomeric α-methyl substituted analogues of 4-(dimethylamino)pyridine: synthesis and evaluation as acyl transfer catalysts
    Alan C. Spivey,Adrian Maddaford,David P. Leese,Alison J. Redgrave J. Chem. Soc. Perkin Trans. 1 2001 1785
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