4-O-tert-ButyldiMethylsilyl Epi Lovastatin

Base Information

Chemical Name:4-O-tert-ButyldiMethylsilyl Epi Lovastatin
CAS No.:82978-03-8
Molecular Formula:C₃₀H₅₀O₅Si
Molecular Weight:518.809
Hs Code.:
Mol file:82978-03-8.mol

Synonyms:4-O-tert-ButyldiMethylsilyl Epi Lovastatin;[1S-[1.alpha.(S*),3.alpha.,7.beta.,8.beta.(2S*,4S*),8a.beta.]]-2-Methyl-butanoic Acid 8-[2-[4-[[(1,1-DiMethylethyl)diMethylsilyl]oxy]tetrahydro-6-oxo-2H-pyran-2-yl]ethyl]-1,2,3,7,8,8a-hexahydro-3,7-diMethyl-1-nap

Suppliers and Price of 4-O-tert-ButyldiMethylsilyl Epi Lovastatin

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
4-O-tert-ButyldimethylsilylEpiLovastatin
2mg
$ 140.00

Biosynth Carbosynth
4-O-tert-Butyldimethylsilyl epi lovastatin
25 mg
$ 1625.00

Biosynth Carbosynth
4-O-tert-Butyldimethylsilyl epi lovastatin
10 mg
$ 810.00

Biosynth Carbosynth
4-O-tert-Butyldimethylsilyl epi lovastatin
5 mg
$ 462.50

Biosynth Carbosynth
4-O-tert-Butyldimethylsilyl epi lovastatin
2 mg
$ 250.00

Biosynth Carbosynth
4-O-tert-Butyldimethylsilyl epi lovastatin
1 mg
$ 150.00

Total 4 raw suppliers

Chemical Property of 4-O-tert-ButyldiMethylsilyl Epi Lovastatin

Chemical Property:

Boiling Point:579.8±50.0 °C(Predicted)
PSA：61.83000
Density:1.03±0.1 g/cm3(Predicted)
LogP:7.22500
Solubility.:Dichloromethane, Dichloromethane, Methanol

Purity/Quality:

97% ^*data from raw suppliers

4-O-tert-ButyldimethylsilylEpiLovastatin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses Protected Lovastatin impurity; an antihypercholesterolemic compound.

Technology Process of 4-O-tert-ButyldiMethylsilyl Epi Lovastatin

There total 16 articles about 4-O-tert-ButyldiMethylsilyl Epi Lovastatin 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%

: 153079-24-4
(S)-2-Methyl-butyric acid (1S,3R,7R,8R,8aR)-8-{2-[(2R,4R)-4-(tert-butyl-dimethyl-silanyloxy)-6-oxo-tetrahydro-pyran-2-yl]-ethyl}-3,7-dimethyl-6-trifluoromethanesulfonyloxy-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl ester

: 79691-11-5,82978-03-8
6(R)-<2-<1,2,6,7,8,8a(R)-Hexahydro-2(S),6(R)-dimethyl-8(S)-<<2(S)-methylbutyryl>oxy>-1(S)-naphtyl>ethyl>-3,4,5,6-tetrahydro-4(R)-<(tert-butyldimethylsilyl)oxy>-2H-pyran-2-one

Guidance literature:: With palladium diacetate; formic acid; tributyl-amine; triphenylphosphine; In N,N-dimethyl-formamide; at 60 ℃; for 1h;
DOI:10.1016/S0040-4039(00)61717-3