Methylglyoxal 1,1-dimethyl acetal

Methylglyoxal 1,1-dimethyl acetal Basic information
Product Name:Methylglyoxal 1,1-dimethyl acetal
Synonyms:PYRUVALDEHYDE DIMETHYLACETAL;PYRUVALDEHYDE 1,1-DIMETHYL ACETAL;PYRUVALDEHYDE-1-DIMETHYL ACETAL;Methylglyoxal dimethyl acetal~Pyruvaldehyde dimethyl acetal;PYRUVIC ALDEHYDE DIMETHYL ACETAL, 97+%;PYRUVIC ALDEHYDE DIMETHYL ACETAL 98%;PYRUVIC ALDEHYDE DIMETHYL ACETAL(INTERMEDIATE OF B-CAROTENE);2-Propanone, 1,1-dimethoxy- (9CI)
CAS:6342-56-9
MF:C5H10O3
MW:118.13
EINECS:228-735-4
Product Categories:ACETYLGROUP;Aldehydes;blocks;BuildingBlocks;ketone;(intermediate of -carotene)
Mol File:6342-56-9.mol
Methylglyoxal 1,1-dimethyl acetal Structure
Methylglyoxal 1,1-dimethyl acetal Chemical Properties
Melting point -57 °C
Boiling point 143-147 °C(lit.)
density 0.976 g/mL at 25 °C(lit.)
vapor pressure 11hPa at 20℃
refractive index n20/D 1.398(lit.)
Fp 100 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
form Liquid
color Clear colorless to yellow
Water Solubility MISCIBLE
BRN 1560557
InChIKeyULVSHNOGEVXRDR-UHFFFAOYSA-N
LogP-0.199 (est)
CAS DataBase Reference6342-56-9
NIST Chemistry Reference2-Propanone, 1,1-dimethoxy-(6342-56-9)
EPA Substance Registry System2-Propanone, 1,1-dimethoxy- (6342-56-9)
Safety Information
Hazard Codes Xi
Risk Statements 10-36/38
Safety Statements 26-36-16
RIDADR UN 1224 3/PG 3
WGK Germany 1
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29145000
MSDS Information
ProviderLanguage
1,1-Dimethoxyacetone English
SigmaAldrich English
ACROS English
ALFA English
Methylglyoxal 1,1-dimethyl acetal Usage And Synthesis
Chemical Propertiesclear colorless to yellow liquid
UsesMethylglyoxal 1,1-dimethyl acetal was used in the synthesis of methylglyoxal via hydrolysis in the presence of H2SO4. It was used to investigate the effects of methylglyoxal-mediated glycation on the structure, thermal stability and enzyme activity of yeast enolase in vivo.
UsesPyruvic Aldehyde Dimethyl Acetal is used in the preparation of MCL1 inhibitors S63845 which is tolerable and effective in diverse cancer models. Also, acts as a synthetic reagent for the preparation of 8novel 2,4-disubstituted pyrimidines as potent, selective, and cell-permeable inhibitors of neuronal nitric oxide synthase. Selective inhibition of neuronal nitric oxide synthase is an important therapeutic approach to target neurodegenerative disorders.
Synthesis Reference(s)The Journal of Organic Chemistry, 41, p. 2642, 1976 DOI: 10.1021/jo00877a030
Methylglyoxal 1,1-dimethyl acetal Methylglyoxal Diphenyldimethoxysilane 4-Chlorobutanal dimethyl acetal 2,2-Dimethoxyethylamine 1-Nonanal Paraldehyde Dimethyldimethoxysilane Acetylacetaldehyde dimethyl acetal 4-Methoxyphenylacetone Acetal 1,1-Dimethoxyethane Bromoacetaldehyde dimethyl acetal Benzaldehyde dimethyl acetal 1,1,2-Trimethoxyethane Methoxyacetone Benzhydrol Propiophenone Methylglyoxal Dimethyl Acetal

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