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Home Halogens 2,3-Dibromopropene, tech grade

2,3-Dibromopropene, tech grade

CAS No.:
513-31-5
Catalog Number:
AG0032XJ
Molecular Formula:
C3H4Br2
Molecular Weight:
199.8719
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%(GC)
In Stock USA
United States
$41
- +
5g
95%(GC)
In Stock USA
United States
$66
- +
25g
90%
In Stock USA
United States
$75
- +
500g
90%
In Stock USA
United States
$750
- +
Product Description
Catalog Number:
AG0032XJ
Chemical Name:
2,3-Dibromopropene, tech grade
CAS Number:
513-31-5
Molecular Formula:
C3H4Br2
Molecular Weight:
199.8719
MDL Number:
MFCD00000211
IUPAC Name:
2,3-dibromoprop-1-ene
InChI:
InChI=1S/C3H4Br2/c1-3(5)2-4/h1-2H2
InChI Key:
YMFWYDYJHRGGPF-UHFFFAOYSA-N
SMILES:
BrCC(=C)Br
EC Number:
208-155-8
UNII:
8DNE7K7Z6P
NSC Number:
6200
Properties
Complexity:
40.2  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
199.866g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
199.873g/mol
Monoisotopic Mass:
197.868g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  
Literature
Title Journal
Formal synthesis of (+/-)-platensimycin. Organic letters 20070426
Identification of glutathione conjugates of 2, 3-dibromopropene in male ICR mice. Archives of pharmacal research 20060201
Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams. The Journal of organic chemistry 20050401
Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions. The Journal of organic chemistry 20040206
Haloalkane dehalogenase LinB from Sphingomonas paucimobilis UT26: X-ray crystallographic studies of dehalogenation of brominated substrates. Biochemistry 20030902
Controlling chemoselectivity in vinyl and allylic C-X bond activation with palladium catalysis: a pK(a)-based electronic switch. Journal of the American Chemical Society 20020220
Properties