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Home Halogens 2,3-Bis(bromomethyl)quinoxaline

2,3-Bis(bromomethyl)quinoxaline

CAS No.:
3138-86-1
Catalog Number:
AG003FG9
Molecular Formula:
C10H8Br2N2
Molecular Weight:
315.9919
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Product Description
Catalog Number:
AG003FG9
Chemical Name:
2,3-Bis(bromomethyl)quinoxaline
CAS Number:
3138-86-1
Molecular Formula:
C10H8Br2N2
Molecular Weight:
315.9919
MDL Number:
MFCD00006729
IUPAC Name:
2,3-bis(bromomethyl)quinoxaline
InChI:
InChI=1S/C10H8Br2N2/c11-5-9-10(6-12)14-8-4-2-1-3-7(8)13-9/h1-4H,5-6H2
InChI Key:
LHKFFORGJVELPC-UHFFFAOYSA-N
SMILES:
BrCc1nc2ccccc2nc1CBr
EC Number:
221-538-4
UNII:
MK7CU7QW5H
NSC Number:
38602
Properties
Complexity:
169  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
315.903g/mol
Formal Charge:
0
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
315.996g/mol
Monoisotopic Mass:
313.905g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
25.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4  
Literature
Title Journal
Synthesis and antimicrobial activity of 2,3-bis(bromomethyl)quinoxaline derivatives. Bioorganic chemistry 20120101
Synthesis and characterization of diiron dithiolate complexes containing a quinoxaline bridge. Dalton transactions (Cambridge, England : 2003) 20111107
An improved understanding of the reaction of bis(bromomethyl)quinoxaline 1-N-oxides with amines using substituent effects. The Journal of organic chemistry 20070427
Controlling the outcome of an N-alkylation reaction by using N-oxide functional groups. The Journal of organic chemistry 20050624
Properties