Ethyl, 1-carboxy-1-hydroxy-

Base Information

Chemical Name:Ethyl, 1-carboxy-1-hydroxy-
CAS No.:15552-92-8
Molecular Formula:C₃H₅O₃
Molecular Weight:89.0709
Hs Code.:

Synonyms:

Suppliers and Price of Ethyl, 1-carboxy-1-hydroxy-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Ethyl, 1-carboxy-1-hydroxy-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Ethyl, 1-carboxy-1-hydroxy-

There total 5 articles about Ethyl, 1-carboxy-1-hydroxy- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%

: 50-99-7
D-glucose

: 72-08-2,113-21-3,311-80-8,1927-28-2,15552-92-8,38140-75-9
D-lactate anion

: 56-81-5,25618-55-7,64333-26-2,8013-25-0
glycerol

Guidance literature:: With potassium dihydrogenphosphate; oxygen; magnesium sulfate; In water; at 30 ℃; for 77h; pH=Ca. 3.0; Reagent/catalyst; Time; Microbiological reaction;

Reference yield: 63.0%

: C₈H₁₇O₆P

: 108-91-8,157973-60-9
cyclohexylamine

: C₃H₇O₆P*3C₆H₁₃N

: 72-08-2,113-21-3,311-80-8,1927-28-2,15552-92-8,38140-75-9
D-lactate anion

Guidance literature:: C₈H₁₇O₆P; With trimethylsilyl bromide; In dichloromethane; Inert atmosphere;

With potassium hydroxide; In water;

cyclohexylamine; In water;
DOI:10.1039/b909241b

Reference yield:

: 41656-56-8
(S)-D-lactoylglutathione

: 70-18-8
GLUTATHIONE

: 72-08-2,113-21-3,311-80-8,1927-28-2,15552-92-8,38140-75-9
D-lactate anion

Guidance literature:: With Zn inactive glyoxalase I (Glo₁) enzyme from Pseudomonas aeruginosa; Kinetics; Enzymatic reaction;
DOI:10.1002/chem.201405402