Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Base Information

Chemical Name:Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester
CAS No.:183429-89-2
Molecular Formula:C₆₀H₉₈NO₁₅P
Molecular Weight:1104.41
Hs Code.:

Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Synonyms:Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Suppliers and Price of Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

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 0 raw suppliers

Chemical Property of Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

There total 1 articles about Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester 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: 85.0%

: Hexadecanoic acid (R)-2-[[(1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-tris-(4-methoxy-benzyloxy)-cyclohexyloxy]-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

: 183429-89-2
Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; water; at 24 ℃; for 3h;
DOI:10.1021/jo961226g

Reference yield:

: 108549-23-1
Dibenzyl N,N-diisopropylphosphoramidite

: 183429-89-2
Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

: 183429-92-7
Hexadecanoic acid (R)-2-[[(1R,2R,3S,4R,5R,6S)-3-benzyloxy-2,6-bis-benzyloxymethoxy-4,5-bis-(bis-benzyloxy-phosphoryloxy)-cyclohexyloxy]-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

Guidance literature:: With 1H-tetrazole; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction; 1.) CH₂Cl₂, 24 deg C, 1 h, 2.) CH₂Cl₂, -40 deg C, 1 h;
DOI:10.1021/jo961226g

Reference yield:

: 108549-23-1
Dibenzyl N,N-diisopropylphosphoramidite

: 183429-89-2
Hexadecanoic acid (R)-2-[((1S,2R,3R,4S,5S,6R)-2,6-bis-benzyloxymethoxy-3,4,5-trihydroxy-cyclohexyloxy)-(2-cyano-ethoxy)-phosphoryloxy]-1-hexadecanoyloxymethyl-ethyl ester

: 183429-91-6
2,6-O-bis(benzyloxymethyl)-3,4,5-O-tris(dibenzylphosphoryl)-D-myo-inositol 1-O-(1,2-O-dipalmitoyl)-sn-glyceryl 2-cyanoethyl phosphate

Guidance literature:: With 1H-tetrazole; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction; 1.) CH₂Cl₂, 24 deg C, 1 h, 2.) CH₂Cl₂, -40 deg C, 1 h;
DOI:10.1021/jo961226g