Cas no 847446-55-3 (Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate)

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate structure
847446-55-3 structure
Product Name:Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate
CAS No:847446-55-3
MF:C11H11BrN2O2
MW:283.121241807938
MDL:MFCD09475852
CID:68930
PubChem ID:26369796
Update Time:2024-10-26

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 8-bromo-6-methylimidazo[1,2-a]pyridine-2-carboxylate
    • Ethyl 5-bromo-7-methylimidazo-[1,2-a]pyridine-2-carboxylate
    • ethyl 8-bromo-6-methylH-imidazo[1,2-a]pyridine-2-carboxylate
    • Ethyl 8-bromo-6-methylimidazo[1,2-a]pyridine-2-carboxylate (ACI)
    • Ethyl8-bromo-6-methylimidazo[1,2-a]pyridine-2-carboxylate
    • MFCD09475852
    • AKOS015834449
    • SCHEMBL24737463
    • Ethyl8-bromo-6-methylh-imidazo[1,2-a]pyridine-2-carboxylate
    • DTXSID20649975
    • CS-0089703
    • 847446-55-3
    • Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate
    • MDL: MFCD09475852
    • Inchi: 1S/C11H11BrN2O2/c1-3-16-11(15)9-6-14-5-7(2)4-8(12)10(14)13-9/h4-6H,3H2,1-2H3
    • InChI Key: XSSOLJXZDJFTRQ-UHFFFAOYSA-N
    • SMILES: O=C(C1=CN2C(C(=CC(C)=C2)Br)=N1)OCC

Computed Properties

  • Exact Mass: 282.00000
  • Monoisotopic Mass: 282.00039g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 275
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3.4
  • Topological Polar Surface Area: 43.6?2

Experimental Properties

  • PSA: 43.60000
  • LogP: 2.58190

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-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%

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate Pricemore >>

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Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate Production Method

Production Method 1

Reaction Conditions
1.1 Solvents: 1,2-Dimethoxyethane ,  Water ;  24 h, rt
1.2 Solvents: Ethanol ;  24 h, reflux
1.3 Reagents: Sodium bicarbonate Solvents: Water
Reference
Evaluation of the 2-substituent effect on the reactivity of the 8-haloimidazo[1,2-a]pyridine series towards Suzuki-type cross-coupling reaction
Kazock, Jean-Yves; Enguehard-Gueiffier, Cecile; Thery, Isabelle; Gueiffier, Alain, Bulletin of the Chemical Society of Japan, 2005, 78(1), 154-159

Production Method 2

Reaction Conditions
1.1 Solvents: Ethanol ;  4 h, 80 °C
Reference
Design, synthesis and evaluation of 2, 6, 8-substituted Imidazopyridine derivatives as potent PI3Kα inhibitors
Chen, Rui; Wang, Zhongyuan; Sima, Lijie; Cheng, Hu; Luo, Bilan; et al, Journal of Enzyme Inhibition and Medicinal Chemistry, 2023, 38(1), 2155638/1-2155638/13

Production Method 3

Reaction Conditions
1.1 Solvents: Ethanol ;  15 min, 0 - 5 °C; 12 h, reflux
Reference
Synthesis and biological evaluation of novel imidazo[1,2-a]pyridine-oxadiazole hybrids as anti-proliferative agents: study of microtubule polymerization inhibition and DNA binding
Sigalapalli, Dilep Kumar; Kiranmai, Gaddam; Parimala Devi, G.; Tokala, Ramya; Sana, Sravani; et al, Bioorganic & Medicinal Chemistry, 2021, 43,

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate Raw materials

Ethyl 8-Bromo-6-methylimidazo1,2-apyridine-2-carboxylate Preparation Products

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