Benzenebutanoic acid, a-hydroxy-a-methyl-

Base Information

Chemical Name:Benzenebutanoic acid, a-hydroxy-a-methyl-
CAS No.:4374-63-4
Molecular Formula:C11H14O3
Molecular Weight:194.23
Hs Code.:
Mol file:4374-63-4.mol

Synonyms:α-Oxy-α-methyl-γ-phenyl-buttersaeure;α-(β-Phenaethyl)-milchsaeure;2-Oxy-4-phenyl-butan-carbonsaeure-(2);2-Hydroxy-2-methyl-4-phenyl-buttersaeure;2-Hydroxy-2-methyl-4-phenyl-butyric acid;

Suppliers and Price of Benzenebutanoic acid, a-hydroxy-a-methyl-

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

TRC
2-Hydroxy-2-methyl-4-phenylbutanoicAcid
50mg
$ 155.00

Total 5 raw suppliers

Chemical Property of Benzenebutanoic acid, a-hydroxy-a-methyl-

Chemical Property:

Melting Point:104.5 - 105.5 °C (benzene)
PSA：57.53000
LogP:1.45480

Purity/Quality:

97% ^*data from raw suppliers

2-Hydroxy-2-methyl-4-phenylbutanoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Benzenebutanoic acid, a-hydroxy-a-methyl-

There total 5 articles about Benzenebutanoic acid, a-hydroxy-a-methyl- 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: 77.0%

: 88151-75-1
2-cyano-4-phenylbutan-2-yl diethylphosphate

: 4374-63-4
2-hydroxy-2-methyl-4-phenyl-butyric acid

Guidance literature:: With hydrogenchloride; for 15h; Heating;

Reference yield:

: 2550-26-7
4-Phenyl-2-butanone

: 4374-63-4
2-hydroxy-2-methyl-4-phenyl-butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / lithium diisopropylamide / tetrahydrofuran / 1.17 h / -10 - 22 °C

2: 77 percent / 20percent HCl / 15 h / Heating

With hydrogenchloride; lithium diisopropyl amide; In tetrahydrofuran;

Reference yield:

: 19345-05-2
methyl 5-methyl-2,3-diphenylisoxazolidine-5-carboxylate

: 4374-63-4
2-hydroxy-2-methyl-4-phenyl-butyric acid

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / Pd-C / ethanol

2: KOH / methanol / Heating

With potassium hydroxide; hydrogen; palladium on activated charcoal; In methanol; ethanol;