(R)-2-HYDROXY-4-PHENYLBUTENOIC ACID

Base Information

Chemical Name:(R)-2-HYDROXY-4-PHENYLBUTENOIC ACID
CAS No.:128573-54-6
Molecular Formula:C10H10O3
Molecular Weight:178.18500
Hs Code.:
Mol file:128573-54-6.mol

Synonyms:

Suppliers and Price of (R)-2-HYDROXY-4-PHENYLBUTENOIC ACID

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of (R)-2-HYDROXY-4-PHENYLBUTENOIC ACID

Chemical Property:

Boiling Point:396.9±32.0 °C(Predicted)
PKA:3.59±0.11(Predicted)
PSA：57.53000
Density:1.277±0.06 g/cm3(Predicted)
LogP:1.14530

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (R)-2-HYDROXY-4-PHENYLBUTENOIC ACID

There total 78 articles about (R)-2-HYDROXY-4-PHENYLBUTENOIC ACID 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: 98.0%

: 100-52-7
benzaldehyde

: 127-17-3
2-oxo-propionic acid

: 128573-54-6
C₁₀H₁₀O₃

Guidance literature:: benzaldehyde; 2-oxo-propionic acid; With potassium hydroxide; In methanol; at 0 - 25 ℃; Inert atmosphere;

With hydrogenchloride; glutamate dehydrogenase; ketone reductase enzyme; nicotinamide adenine dinucleotide phosphate; sodium hydroxide; In aq. phosphate buffer; water; at 30 ℃; for 24h; pH=6; Reagent/catalyst; Temperature; Enzymatic reaction;

Reference yield: 90.0%

: 1914-59-6
(E)-2-oxo-4-phenyl-3-butenoic acid

: 140632-55-9,128573-54-6
(R)-(E)-2-hydroxy-4-phenyl-3-butenoic acid

Guidance literature:: With hydrogen; 1,1'-dibenzyl-4,4'-bipyridinium; In water; at 35 ℃; under 760 Torr; Product distribution; Mechanism; Equilibrium constant; other 2-oxo acids; or sodium formate (or both together), biosynthesis by Proteus vulgaris (potassium phosphate buffer pH 7.0), pH dependence, various reaction times, or cell free extract (other reagent, other temperature);
DOI:10.1016/S0040-4020(01)86506-6