(1R,2R)-(thiophen-3-yl)-2,3-glycidol

Base Information

Chemical Name:(1R,2R)-(thiophen-3-yl)-2,3-glycidol
CAS No.:1282033-86-6
Molecular Formula:C₇H₈O₂S
Molecular Weight:156.205
Hs Code.:

Synonyms:

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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 (1R,2R)-(thiophen-3-yl)-2,3-glycidol

Chemical Property:

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Technology Process of (1R,2R)-(thiophen-3-yl)-2,3-glycidol

There total 5 articles about (1R,2R)-(thiophen-3-yl)-2,3-glycidol 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:

: 852998-62-0
α-vinyl-(3-thiophenyl)methanol

: 1282033-73-1,852998-62-0
(R)‐1‐(thiophen‐3‐yl)prop‐2‐en‐1‐ol

: 1282033-86-6
(1R,2R)-(thiophen-3-yl)-2,3-glycidol

Guidance literature:: With whole E_. coli cells expressing monooxygenase from Herbaspirillum huttiense HhMO and NADH-dependent flavin oxidoreductase PsStyB; In aq. phosphate buffer; octane; at 37 ℃; for 0.333333h; pH=6; stereoselective reaction; Resolution of racemate; Green chemistry; Enzymatic reaction;
DOI:10.1039/d0cy00081g

Reference yield:

: 498-62-4
3-thiophene carboxaldehyde

: 1282033-73-1,852998-62-0
(R)‐1‐(thiophen‐3‐yl)prop‐2‐en‐1‐ol

: 1282033-86-6
(1R,2R)-(thiophen-3-yl)-2,3-glycidol

: (1S,2R)-1-(thiophen-3-yl)glycidol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / Cooling

2: Escherichia coli BL₂₁ harboring the plasmid pET₂₈a(+) encoding the styAB gene from Pseudomonas sp. LQ₂₆ / 3 h / pH 6.5 / aq. phosphate buffer; Enzymatic reaction

With Escherichia coli BL₂₁ harboring the plasmid pET₂₈a(+) encoding the styAB gene from Pseudomonas sp. LQ₂₆; In tetrahydrofuran;
DOI:10.1039/c0cc04360e

Reference yield:

: 498-62-4
3-thiophene carboxaldehyde

: 852998-62-0
(S)‐1‐(thiophen‐3‐yl)prop‐2‐en‐1‐ol

: 1282033-73-1,852998-62-0
(R)‐1‐(thiophen‐3‐yl)prop‐2‐en‐1‐ol

: 1-(thiophen-3-yl)glycidol

: 1282033-86-6
(1R,2R)-(thiophen-3-yl)-2,3-glycidol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / Cooling

2: Escherichia coli BL₂₁ harboring the plasmid pET₂₈a(+) encoding the styAB gene from Pseudomonas sp. LQ₂₆ / pH 6.5 / aq. phosphate buffer; Enzymatic reaction

With Escherichia coli BL₂₁ harboring the plasmid pET₂₈a(+) encoding the styAB gene from Pseudomonas sp. LQ₂₆; In tetrahydrofuran;
DOI:10.1039/c0cc04360e