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Home Halogens Ethyl 3-bromo-2-oxopropanoate

Ethyl 3-bromo-2-oxopropanoate

CAS No.:
70-23-5
Catalog Number:
AG0034VY
Molecular Formula:
C5H7BrO3
Molecular Weight:
195.0113
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
25g
95%
In Stock USA
United States
$30
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Product Description
Catalog Number:
AG0034VY
Chemical Name:
Ethyl 3-bromo-2-oxopropanoate
CAS Number:
70-23-5
Molecular Formula:
C5H7BrO3
Molecular Weight:
195.0113
MDL Number:
MFCD00000204
IUPAC Name:
ethyl 3-bromo-2-oxopropanoate
InChI:
InChI=1S/C5H7BrO3/c1-2-9-5(8)4(7)3-6/h2-3H2,1H3
InChI Key:
VICYTAYPKBLQFB-UHFFFAOYSA-N
SMILES:
CCOC(=O)C(=O)CBr
EC Number:
200-729-6
NSC Number:
62182
Properties
Complexity:
121  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
193.958g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
195.012g/mol
Monoisotopic Mass:
193.958g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
43.4A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.2  
Literature
Title Journal
Ethyl 8-amino-6-bromoimidazo[1,2-a]pyridine-2-carb-oxy-late. Acta crystallographica. Section E, Structure reports online 20110601
Ethyl 5-methyl-imidazo[1,2-a]pyridine-2-carboxyl-ate. Acta crystallographica. Section E, Structure reports online 20100801
Calyculins and related marine natural products as serine-threonine protein phosphatase PP1 and PP2A inhibitors and total syntheses of calyculin A, B, and C. Marine drugs 20100101
A one-pot synthesis of functionalized thiazoles from acid chlorides, secondary amines, ethyl bromopyruvate, and ammonium thiocyanate. Molecular diversity 20090801
Variable involvement of the perivascular retinal tissue in carbonic anhydrase inhibitor induced relaxation of porcine retinal arterioles in vitro. Investigative ophthalmology & visual science 20071001
Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction of isocyanides with activated acetylenes in the presence of ethyl bromopyruvate. Molecular diversity 20060801
Properties