rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

Base Information

Chemical Name:rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione
CAS No.:81912-43-8
Molecular Formula:C₂₁H₃₇NO₃S₂
Molecular Weight:415.662
Hs Code.:

Synonyms:rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

Suppliers and Price of rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

There total 1 articles about rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione 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: 92.1%

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 81912-43-8
rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

: 81912-43-8
S-(+)-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

: 81912-47-2
N-n-hexadecanoyl methyl (L)-phenylalaninate

Guidance literature:: With triethylamine; In dichloromethane; for 8h; Product distribution; Relationship between chirality of amine reactant and the asymmetric consumption of acylating thiazolidine;
DOI:10.1016/S0040-4039(00)86786-6

Reference yield: 93.7%

: 81912-43-8
(R)-3-Hexadecanoyl-2-thioxo-thiazolidine-4-carboxylic acid methyl ester

: 24461-61-8,26682-99-5,37760-98-8,6591-61-3
phenylglycine methyl ester

: 80963-80-0
4(S)-(methoxycarbonyl)-1,3-thiazolidine-2-thione

: 81912-46-1
(S)-Hexadecanoylamino-phenyl-acetic acid methyl ester

Guidance literature:: In dichloromethane; for 12h; Product distribution; Ambient temperature; Asymmetric amidation of racemic amines by optically active acylthiazolidines. E_.e. of products 0.2-64.4percent; solvent effect.;
DOI:10.1016/S0040-4039(00)86785-4

Reference yield: 92.1%

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 81912-43-8
rac.-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

: 81912-43-8
S-(+)-3-hexadecanoyl-4-methoxycarbonyl-1,3-thiazolidine-2-thione

: 81912-47-2
N-n-hexadecanoyl methyl (L)-phenylalaninate

Guidance literature:: With triethylamine; In dichloromethane; for 8h; Product distribution; Relationship between chirality of amine reactant and the asymmetric consumption of acylating thiazolidine;
DOI:10.1016/S0040-4039(00)86786-6