1. Home
  2. Imidazo[1,2-b]pyridazine, 3-bromo-6-chloro-2-methyl-

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-b]pyridazine, 3-bromo-6-chloro-2-methyl-

Clc1ccc2n(n1)c(Br)c(n2)C Request for Quotation
Chemical Name: Imidazo[1,2-b]pyridazine, 3-bromo-6-chloro-2-methyl-
CAS Number: 18112-31-7
Product Number: AG0022PF(AGN-PC-00NO54)
Synonyms:
MDL No:
Molecular Formula: C7H5BrClN3
Molecular Weight: 246.4917

Identification/Properties

Computed Properties
Molecular Weight:
246.492g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
244.936g/mol
Monoisotopic Mass:
244.936g/mol
Topological Polar Surface Area:
30.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
180
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine plays a crucial role in chemical synthesis as a versatile building block. This compound serves as a key intermediate in the creation of various biologically active molecules and pharmaceuticals. Its unique structure imparts valuable reactivity in organic reactions, enabling the formation of intricate molecular frameworks. In particular, the presence of bromine and chlorine substituents in conjunction with the imidazo[1,2-b]pyridazine scaffold offers a wide range of chemoselective functionalization pathways. Chemists utilize this compound in the synthesis of novel drug candidates, agrochemicals, and materials with tailored properties. Its strategic incorporation into synthetic routes allows for the rapid construction of diverse molecular architectures, making it a valuable tool in the field of chemical synthesis.