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14519-10-9

14519-10-9 | Bromamide (6CI,7CI,8CI,9CI)

CAS No: 14519-10-9 Catalog No: AG001KNO MDL No:

Product Description

Catalog Number:
AG001KNO
Chemical Name:
Bromamide (6CI,7CI,8CI,9CI)
CAS Number:
14519-10-9
Molecular Formula:
BrH2N
Molecular Weight:
95.9266
InChI:
InChI=1S/BrH2N/c1-2/h2H2
InChI Key:
FNXLCIKXHOPCKH-UHFFFAOYSA-N
SMILES:
NBr

Properties

Complexity:
2  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
94.937g/mol
Formal Charge:
0
Heavy Atom Count:
2  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
95.927g/mol
Monoisotopic Mass:
94.937g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
26A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  

Literature

Title Journal
Cross-linking methionine and amine residues with reactive halogen species. Free radical biology & medicine 20140501
Evaluation of pretreatments for inhibiting bromate formation during ozonation. Environmental technology 20120101
Hypobromous acid and bromamine production by neutrophils and modulation by superoxide. The Biochemical journal 20090201
The vinyl ether linkages of plasmalogens are favored targets for myeloperoxidase-derived oxidants: a kinetic study. Biochemistry 20080805
Cyanogen bromide formation from the reactions of monobromamine and dibromamine with cyanide ion. Environmental science & technology 20060415
A sensitive and selective assay for chloramine production by myeloperoxidase. Free radical biology & medicine 20051201
The role of reactive N-bromo species and radical intermediates in hypobromous acid-induced protein oxidation. Free radical biology & medicine 20051001
Bromamine decomposition kinetics in aqueous solutions. Environmental science & technology 20040401
Oxidation of NADH by chloramines and chloramides and its activation by iodide and by tertiary amines. Archives of biochemistry and biophysics 20010915
The eosinophil peroxidase-hydrogen peroxide-bromide system of human eosinophils generates 5-bromouracil, a mutagenic thymine analogue. Biochemistry 20010220

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