Glyoxylic acid monohydrate - CAS 563-96-2

Name: Glyoxylic acid monohydrate
Brand: BOC Sciences
Rating: 5 (1 reviews)

Catalog:	BB029349
Product Name:	Glyoxylic acid monohydrate
CAS:	563-96-2
Synonyms:	oxaldehydic acid;hydrate

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	oxaldehydic acid;hydrate
Description:	Occurs in unripe fruit and in young green leaves; has also been found in very young sugar beets.
Molecular Weight:	92.05
Molecular Formula:	C2H4O4
Canonical SMILES:	C(=O)C(=O)O.O
InChI:	InChI=1S/C2H2O3.H2O/c3-1-2(4)5;/h1H,(H,4,5);1H2
InChI Key:	MOOYVEVEDVVKGD-UHFFFAOYSA-N
Boiling Point:	100 °C
Purity:	98 %
Density:	1.33 g/cm³
Appearance:	White to light yellow crystalline powder or chunks
MDL:	MFCD00149497
LogP:	-0.79440

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Related Functional Groups

Carbonyl Compounds

[89908-23-6]C23H22N2O5
2-Propenoic acid, 2-(3',3'-dimethyl-6-nitrospiro[2H-1-benzopyran-2,2'-[2H]indol]-1'(3'H)-yl)ethyl ester
[51493-02-8]C5H10ClNO
N-Methyl-N-propylcarbamoyl Chloride
[35153-16-3]C16H30O2
(Z)-10-Tetradecenyl Acetate
[1018141-88-2]C17H14N4O2
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[1035840-45-9]C14H16N2O4
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid
[956439-56-8]C6H5N3O6
1-(Carboxymethyl)-3-nitro-1H-pyrazole-5-carboxylic acid

GHS Hazard Statement:	H314 (15.38%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
Precautionary Statement:	P260, P261, P264, P272, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P333+P313, P363, P405, and P501
Signal Word:	Danger

Publication Number	Title	Priority Date
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CN-113354810-A	Clustering peptide with side chain containing functionalized biphenyl group and preparation method thereof	20210607
CN-112940291-A	Transparent hydrogel based on chitosan and preparation method thereof	20210205
CN-112851708-A	Method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and diphosphine ligand used by method	20210119
CN-112745336-A	Preparation method of anti-infection cephalosporin drug	20201227

PMID	Publication Date	Title	Journal
18715040	20081101	Efficient ytterbium triflate catalyzed microwave-assisted synthesis of 3-acylacrylic acid building blocks	Journal of combinatorial chemistry
18802603	20081007	Oxidative decarboxylative synthesis of 2-H-imidazolines from glyoxylic acid and 1,2-diamines	Chemical communications (Cambridge, England)
18294852	20080315	Synthesis and structure-activity relationship studies in peripheral benzodiazepine receptor ligands related to alpidem	Bioorganic & medicinal chemistry
16018658	20050721	A two-stage iterative process for the synthesis of poly-oxazoles	Organic letters
15724206	20050114	Novel alpha-functionally substituted amino acids: diphenylphosphinoglycines	Chemical communications (Cambridge, England)

Complexity:	55.9
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	2
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	92.01095860
Formal Charge:	0
Heavy Atom Count:	6
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	92.01095860
Rotatable Bond Count:	1
Topological Polar Surface Area:	55.4 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0