Cas no 887602-89-3 (Methyl indolizine-7-carboxylate)

Methyl indolizine-7-carboxylate is a versatile heterocyclic compound featuring an indolizine core esterified at the 7-position. This structure imparts unique reactivity, making it a valuable intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. The ester functional group enhances solubility and facilitates further derivatization, such as hydrolysis or amidation. Its rigid bicyclic framework contributes to stability while offering opportunities for structural diversification. The compound is often employed in the development of bioactive molecules due to its potential for modulating electronic and steric properties. High purity grades are available to ensure reproducibility in research and industrial applications.
Methyl indolizine-7-carboxylate structure
887602-89-3 structure
Product Name:Methyl indolizine-7-carboxylate
CAS No:887602-89-3
MF:C10H9NO2
MW:175.183962583542
MDL:MFCD10566763
CID:713992
PubChem ID:44558556
Update Time:2025-10-13

Methyl indolizine-7-carboxylate Chemical and Physical Properties

Names and Identifiers

    • Methyl indolizine-7-carboxylate
    • 7-Indolizinecarboxylicacid, methyl ester
    • Methyl indolizine-7-carboxylate
    • 7-Indolizinecarboxylic acid, methyl ester
    • FCH881118
    • 7-Indolizinecarboxylicacid,methyl ester
    • 7-indolizinecarboxylic acid methyl ester
    • OR301176
    • SY027259
    • AX8139470
    • AB0027354
    • ST24031193
    • W9179
    • A842888
    • Methyl 7-indolizinecarboxylate (ACI)
    • MFCD10566763
    • J-522609
    • AKOS006305285
    • DTXSID70659443
    • FS-2967
    • CS-W003729
    • 887602-89-3
    • SCHEMBL21816172
    • MDL： MFCD10566763
    • Inchi： 1S/C10H9NO2/c1-13-10(12)8-4-6-11-5-2-3-9(11)7-8/h2-7H,1H3
    • InChI Key： BVQIGDNWKHPLOE-UHFFFAOYSA-N
    • SMILES： O=C(C1=CC2N(C=CC=2)C=C1)OC

Computed Properties

  • Exact Mass: 175.06300
  • Monoisotopic Mass: 175.063
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 205
  • 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
  • Topological Polar Surface Area: 30.7
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.4

Experimental Properties

  • Color/Form: No data available
  • Density: 1.16
  • Melting Point: No data available
  • Boiling Point: No data available
  • Flash Point: No data available
  • Refractive Index: 1.573
  • PSA: 30.71000
  • LogP: 1.72590

Methyl indolizine-7-carboxylate Security Information

Methyl indolizine-7-carboxylate Customs Data

  • HS CODE：2933990090
  • Customs Data：

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Methyl indolizine-7-carboxylate Pricemore >>

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Methyl indolizine-7-carboxylate Production Method

Production Method 1

Reaction Conditions
1.1 Catalysts: Tributylphosphine Solvents: Acetonitrile ;  2 - 8 h, 20 - 25 °C
Reference
Phosphines catalyzed nucleophilic addition of azoles to allenes: synthesis of allylazoles and indolizines
Virieux, David; Guillouzic, Anne-Francoise; Cristau, Henri-Jean, Tetrahedron, 2006, 62(15), 3710-3720

Methyl indolizine-7-carboxylate Raw materials

Methyl indolizine-7-carboxylate Preparation Products

Methyl indolizine-7-carboxylate Related Literature

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