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Home Aldehydes 2-Bromomalonaldehyde

2-Bromomalonaldehyde

CAS No.:
2065-75-0
Catalog Number:
AG00336L
Molecular Formula:
C3H3BrO2
Molecular Weight:
150.9587
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$8
- +
25g
95%
In Stock USA
United States
$19
- +
100g
95%
In Stock USA
United States
$50
- +
500g
95%
In Stock USA
United States
$165
- +
Product Description
Catalog Number:
AG00336L
Chemical Name:
2-Bromomalonaldehyde
CAS Number:
2065-75-0
Molecular Formula:
C3H3BrO2
Molecular Weight:
150.9587
MDL Number:
MFCD00459999
IUPAC Name:
2-bromopropanedial
InChI:
InChI=1S/C3H3BrO2/c4-3(1-5)2-6/h1-3H
InChI Key:
SURMYNZXHKLDFO-UHFFFAOYSA-N
SMILES:
O=CC(C=O)Br
Properties
Complexity:
53.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
149.932g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
150.959g/mol
Monoisotopic Mass:
149.932g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
34.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  
Literature
Title Journal
1-{4-Chloro-2-[2-(2-fluoro-phen-yl)-1,3-dithio-lan-2-yl]phen-yl}-2-methyl-1H-imidazole-5-carbaldehyde. Acta crystallographica. Section E, Structure reports online 20110201
2-Chloro-6,6-dimethyl-5,6-dihydro-indazolo[2,3-c]quinazoline. Acta crystallographica. Section E, Structure reports online 20100301
Solid-phase synthesis of 4(5),1',5'-trisubstituted 2,4'-biimidazoles. The Journal of organic chemistry 20091218
Reaction routes leading to CO2 and CO in the Briggs-Rauscher oscillator: analogies between the oscillatory BR and BZ reactions. The journal of physical chemistry. A 20090813
Solid-phase synthesis of 7-substituted 3H-imidazo[2,1-i]purines. Organic & biomolecular chemistry 20061221
Reactions of 9-substituted guanines with bromomalondialdehyde in aqueous solution predominantly yield glyoxal-derived adducts. Organic & biomolecular chemistry 20040707
New nucleoside analogs from 2-amino-9-(beta-D-ribofuranosyl)purine. Organic & biomolecular chemistry 20040321
Properties