1. Home
  2. Imidazo[1,2-a]pyridine-3-acetonitrile, 2-methyl-8-(phenylmethoxy)-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Imidazo[1,2-a]pyridine-3-acetonitrile, 2-methyl-8-(phenylmethoxy)-

N#CCc1c(C)nc2n1cccc2OCc1ccccc1 Request for Quotation
Chemical Name: Imidazo[1,2-a]pyridine-3-acetonitrile, 2-methyl-8-(phenylmethoxy)-
CAS Number: 76081-98-6
Product Number: AG00G2EO(AGN-PC-073SG8)
Synonyms:
MDL No: MFCD00834620
Molecular Formula: C17H15N3O
Molecular Weight: 277.3205

Identification/Properties

Computed Properties
Molecular Weight:
277.327g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
277.122g/mol
Monoisotopic Mass:
277.122g/mol
Topological Polar Surface Area:
50.3A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
385
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


SCH 28080 is a potent inhibitor of the calcium pump ATPase in the sarcoplasmic reticulum of cardiac muscle cells. This compound is commonly utilized in chemical synthesis as a critical tool for probing calcium-dependent processes within cellular systems. By specifically targeting the calcium pump ATPase, SCH 28080 effectively disrupts the transport of calcium ions across the membrane, leading to a more comprehensive understanding of the role of calcium signaling in various biological pathways. In chemical synthesis, the precise modulation of calcium levels using SCH 28080 can provide valuable insights into the mechanisms of action of numerous enzymes and signaling molecules, thereby advancing innovative approaches for the development of novel pharmaceuticals and bioactive compounds.