(R)-ethyl 3,4-dihydroxybutanoate

Base Information

Chemical Name:(R)-ethyl 3,4-dihydroxybutanoate
CAS No.:108585-47-3
Molecular Formula:C₆H₁₂O₄
Molecular Weight:148.159
Hs Code.:
Mol file:108585-47-3.mol

Synonyms:

Suppliers and Price of (R)-ethyl 3,4-dihydroxybutanoate

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
(3S)-3,4-DihydroxybutanoicAcidEthylEster(~90%)
50mg
$ 145.00

TRC
(3S)-3,4-DihydroxybutanoicAcidEthylEster(~90%)
500mg
$ 1135.00

ChemScene
Butanoicacid,3,4-dihydroxy-,ethylester,(3S)-
1g
$ 715.00

American Custom Chemicals Corporation
(S)-ETHYL-3,4-DIHYDROXYBUTANOATE 95.00%
5MG
$ 501.26

Total 6 raw suppliers

Chemical Property of (R)-ethyl 3,4-dihydroxybutanoate

Chemical Property:

Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly)

Purity/Quality:

98%Min ^*data from raw suppliers

(3S)-3,4-DihydroxybutanoicAcidEthylEster(~90%) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses (3S)-3,4-Dihydroxybutanoic Acid Ethyl Ester is used in the synthesis of laulimalide anti-tumor agents.

Technology Process of (R)-ethyl 3,4-dihydroxybutanoate

There total 9 articles about (R)-ethyl 3,4-dihydroxybutanoate 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%

: 691-84-9
Diethyl (S)-malate

: 112635-76-4,108585-47-3
(S)-ethyl 3,4-dihydroxybutanoate

Guidance literature:: Diethyl (S)-malate; With dimethylsulfide borane complex; In tetrahydrofuran; for 1h; Inert atmosphere;

With sodium tetrahydroborate; In tetrahydrofuran; at 0 - 25 ℃; for 12h; Inert atmosphere;
DOI:10.1002/ejoc.202001563

Reference yield: 92.0%

: 32223-97-5
(+/-)-ethyl-3,4-epoxybutanoate

: 112083-64-4
ethyl 2-((2R)-oxiran-2-yl)acetate

: 112635-76-4,108585-47-3
(S)-ethyl 3,4-dihydroxybutanoate

Guidance literature:: With (1R,2R)-(-)-N,N'-bis(3,5-di-tert-butylsalicydene)-1,2-cyclohexanediaminocobalt(II); air; acetic acid; In tetrahydrofuran; at 0 - 20 ℃; for 16h;
DOI:10.1021/ja016737l

Reference yield: 90.0%

: 85518-49-6
ethyl γ-hydroxyacetoacetate

: 112635-76-4,108585-47-3
(S)-ethyl 3,4-dihydroxybutanoate

Guidance literature:: With D-glucose; broth E_. coli HB₁₀₁; pNTS₁G; NADP; In various solvent(s); at 30 ℃; for 20h; pH=6.5; Enzymatic reaction;
DOI:10.1016/S0957-4166(01)00279-8