(S)-hept-1-yn-3-yl acetate

Base Information

Chemical Name:(S)-hept-1-yn-3-yl acetate
CAS No.:200504-46-7
Molecular Formula:C₉H₁₄O₂
Molecular Weight:154.209
Hs Code.:

Synonyms:

Suppliers and Price of (S)-hept-1-yn-3-yl acetate

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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)-hept-1-yn-3-yl acetate

Chemical Property:

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Technology Process of (S)-hept-1-yn-3-yl acetate

There total 5 articles about (S)-hept-1-yn-3-yl acetate 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: 49.0%

: 108-05-4,9003-20-7
vinyl acetate

: 7383-19-9
hept-1-yn-3-ol

: 51703-65-2,7383-19-9,51586-58-4,51703-66-3
(R)-1-heptyn-3-ol

: 200504-46-7
(S)-hept-1-yn-3-yl acetate

Guidance literature:: With Novozyme 435; In pentane; at 20 ℃; Molecular sieve; Enzymatic reaction;
DOI:10.1002/adsc.202000404

Reference yield: 40.0%

: 108-05-4,9003-20-7
vinyl acetate

: 7383-19-9
hept-1-yn-3-ol

: 51703-66-3
(S)-(-)-1-heptyn-3-ol

: 51703-65-2,7383-19-9,51586-58-4,51703-66-3
(R)-1-heptyn-3-ol

: 200504-46-7
(S)-hept-1-yn-3-yl acetate

Guidance literature:: With Novozym 435; In di-isopropyl ether; at 20 ℃; for 5h; optical yield given as %ee; enantioselective reaction; Enzymatic reaction;
DOI:10.1271/bbb.110206

Reference yield:

: 108-05-4,9003-20-7
vinyl acetate

: 7383-19-9
hept-1-yn-3-ol

: 51703-65-2,7383-19-9,51586-58-4,51703-66-3
(R)-1-heptyn-3-ol

: 65253-18-1
(R)-hept-1-yn-3-yl acetate

: 200504-46-7
(S)-hept-1-yn-3-yl acetate

Guidance literature:: With Mycobacterium smegmatis acyl transferase; In aq. phosphate buffer; at 21 ℃; for 2h; pH=7.5; enantioselective reaction; Inert atmosphere; Resolution of racemate; Enzymatic reaction;
DOI:10.1002/adsc.201701282