,S^)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Base Information

Chemical Name:*,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate
CAS No.:121441-83-6
Molecular Formula:C₂₇H₃₆O₄S
Molecular Weight:456.646
Hs Code.:

<R-(R<sup>*</sup>,S<sup>*</sup>)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Synonyms:*,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Suppliers and Price of *,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

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

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Chemical Property of *,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Chemical Property:

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Technology Process of *,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

There total 2 articles about *,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate 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:

: 121441-81-4,121521-50-4,121521-51-5
Methyl 2-methoxy-3-hydroxy-3-[2-(8-phenyloctyl)phenyl ]propanoate

: 507-09-5
tiolacetic acid

: 121441-82-5
(Z)-methyl 2-methoxy-3-<2-(8-phenyloctyl)phenyl>-2-propenoate

: (2R,3S)-3-Acetylsulfanyl-2-methoxy-3-[2-(8-phenyl-octyl)-phenyl]-propionic acid methyl ester

: 121441-83-6,121521-52-6,121521-53-7
(R^*,R^*)-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Guidance literature:: With tributylphosphine; di-isopropyl azodicarboxylate; Multistep reaction. Title compound not separated from byproducts; 1.) toluene, 45 min.,2.) toluene, 18 h, room temp.;
DOI:10.1021/jo00275a045

Reference yield:

: 121441-81-4
*,S^*)>-methyl β-hydroxy-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

: 507-09-5
tiolacetic acid

: 121441-82-5
(Z)-methyl 2-methoxy-3-<2-(8-phenyloctyl)phenyl>-2-propenoate

: 121441-83-6
*,S^*)>-methyl β-(acethylthio)-α-methoxy-2-(8-phenyloctyl)benzenepropanoate

Guidance literature:: With tributylphosphine; di-isopropyl azodicarboxylate; Yield given. Multistep reaction. Yields of byproduct given; 1.) toluene, 45 min, 2.) toluene, 18 h, room temp.;
DOI:10.1021/jo00275a045