Home Carboxys 2,3-Oxiranedicarboxylic acid

2,3-Oxiranedicarboxylic acid

CAS No.:
3272-11-5
Catalog Number:
AG01FNQI
Molecular Formula:
C4H4O5
Molecular Weight:
132.0716
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Product Description
Catalog Number:
AG01FNQI
Chemical Name:
2,3-Oxiranedicarboxylic acid
CAS Number:
3272-11-5
Molecular Formula:
C4H4O5
Molecular Weight:
132.0716
MDL Number:
MFCD00070513
IUPAC Name:
oxirane-2,3-dicarboxylic acid
InChI:
InChI=1S/C4H4O5/c5-3(6)1-2(9-1)4(7)8/h1-2H,(H,5,6)(H,7,8)
InChI Key:
DCEMCPAKSGRHCN-UHFFFAOYSA-N
SMILES:
OC(=O)C1OC1C(=O)O
NSC Number:
243799
Properties
Complexity:
144  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
132.006g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
132.071g/mol
Monoisotopic Mass:
132.006g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
87.1A^2
Undefined Atom Stereocenter Count:
2  
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.9  
Literature
Title Journal
Structure-based development of specific inhibitors for individual cathepsins and their medical applications. Proceedings of the Japan Academy. Series B, Physical and biological sciences 20110210
Calpains: attractive targets for the development of synthetic inhibitors. Current topics in medicinal chemistry 20100101
Structures of falcipain-2 and falcipain-3 bound to small molecule inhibitors: implications for substrate specificity. Journal of medicinal chemistry 20090212
[Extraction of Pb from sewage sludge with PESA]. Huan jing ke xue= Huanjing kexue 20080101
Isolation and characterization of a new bacterium capable of biotransforming cis -epoxysuccinic acid to D(-) -tartaric acid. FEMS microbiology letters 20070201
Flow calorimetry--a useful tool for determination of immobilized cis-epoxysuccinate hydrolase activity from Nocardia tartaricans. Artificial cells, blood substitutes, and immobilization biotechnology 20040201
Aza-peptide epoxides: potent and selective inhibitors of Schistosoma mansoni and pig kidney legumains (asparaginyl endopeptidases). Biological chemistry 20031201
Properties