2-(Isopropylamino)-2-oxoacetic Acid - CAS 29262-57-5

Catalog:	BB020153
Product Name:	2-(Isopropylamino)-2-oxoacetic Acid
CAS:	29262-57-5
Synonyms:	2-oxo-2-(propan-2-ylamino)acetic acid; 2-oxo-2-(propan-2-ylamino)acetic acid

Technical Data

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Computed Properties

IUPAC Name:	2-oxo-2-(propan-2-ylamino)acetic acid
Description:	2-(Isopropylamino)-2-oxoacetic Acid (CAS# 29262-57-5) is a useful research chemical.
Molecular Weight:	131.13
Molecular Formula:	C5H9NO3
Canonical SMILES:	CC(C)NC(=O)C(=O)O
InChI:	InChI=1S/C5H9NO3/c1-3(2)6-4(7)5(8)9/h3H,1-2H3,(H,6,7)(H,8,9)
InChI Key:	KBMFHCMLHQGQEB-UHFFFAOYSA-N
Density:	1.17 g/cm³
MDL:	MFCD06740186
LogP:	-0.01350

Publication Number	Title	Priority Date
US-2015335674-A1	Ldh inhibitors as treatment for fibrosis and fibrotic-related disorders	20140521
US-10329263-B2	Disubstituted 1, 2, 4-triazine compound	20140424
US-2016272640-A1	Substituted piperidin-4-amino-type compounds and uses thereof	20121227
EP-2168957-B1	Alkyl-substituted tetrahydropyranes as aromatic materials	20090306
AU-2007334659-A1	Indazolyl ester and amide derivatives for the treatment of glucocorticoid receptor mediated disorders	20061221

PMID	Publication Date	Title	Journal
21946930	20111201	Exogenous pyruvate accelerates glycolysis and promotes capacitation in human spermatozoa	Human reproduction (Oxford, England)
15968824	20050401	Trypanocidal activity of N-isopropyl oxamate on cultured epimastigotes and murine trypanosomiasis using different Trypanosoma cruzi strains	Journal of enzyme inhibition and medicinal chemistry
14506918	20030601	Inhibition of Trypanosoma cruzi alpha-hydroxyacid dehydrogenase-isozyme II by N-isopropyl oxamate and its effect on intact epimastigotes	Journal of enzyme inhibition and medicinal chemistry
15051959	20030101	Inhibition of lactate dehydrogenase C4 (LDH-C4) blocks capacitation of mouse sperm in vitro	Cytogenetic and genome research
12434572	20020101	The study of N-isopropyl oxamate on sperm motility and fertility, in mice	Proceedings of the Western Pharmacology Society

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Related Functional Groups

Carbonyl Compounds

[89908-23-6]
2-Propenoic acid, 2-(3',3'-dimethyl-6-nitrospiro[2H-1-benzopyran-2,2'-[2H]indol]-1'(3'H)-yl)ethyl ester
[5650-34-0]
Oxiran-2-yl(phenyl)methanone
[1383427-98-2]
(S)-Hexahydropyrazino[2,1-c][1,4]oxazin-4(3H)-one hydrochloride
[70199-62-1]
(4-Pyridyl)acetone Hydrochloride
[35153-16-3]
(Z)-10-Tetradecenyl Acetate
[55441-25-3]
1-(2-Cyanophenyl)urea

GHS Hazard Statement:	H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	130
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	131.058243149
Formal Charge:	0
Heavy Atom Count:	9
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	131.058243149
Rotatable Bond Count:	2
Topological Polar Surface Area:	66.4 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	0.3