BEA₃₈₈

Base Information

Chemical Name:BEA₃₈₈
CAS No.:214139-27-2
Molecular Formula:C₃₅H₄₃N₃O₈
Molecular Weight:633.742
Hs Code.:

Synonyms:

Suppliers and Price of BEA₃₈₈

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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 BEA₃₈₈

Chemical Property:

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Technology Process of BEA₃₈₈

There total 7 articles about BEA₃₈₈ 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:

: 7480-35-5,13286-59-4,74165-73-4,126456-43-7,136030-00-7,140632-19-5,140632-20-8
(1S,2R)-1-amino-2-indanol

: 214139-27-2
BEA₃₈₈

Guidance literature:: Multi-step reaction with 3 steps

1.1: Et₃N / methanol / 1.17 h / 20 °C

1.2: 83 percent / pyridine / 16 h / 20 °C

2.1: 65 percent / NaOMe / methanol; CH₂Cl₂ / 5 h / pH 7.5

With sodium methylate; triethylamine; In methanol; dichloromethane; 1.1: Condensation / 1.2: Acetylation / 2.1: Deacetylation;
DOI:10.1139/v00-012

Reference yield:

: 213895-58-0
2,5-di-O-benzyl-L-mannaro-1,4:3,6-di-γ-lactone

: 214139-27-2
BEA₃₈₈

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / 2-hydroxypyridine / tetrahydrofuran; CHCl₃ / 0.25 h / 20 °C

2: 85 percent / camphorsulfonic acid / acetone / 0.25 h

3: N₂O₄; Pb(NO₃)2; NaOAc / CH₂Cl₂ / 1.5 h / -60 - -10 °C

4: 100 percent / 30 percent aq. H₂O₂; LiOH / tetrahydrofuran / 0.33 h / 0 °C

With 2-hydroxypyridin; lithium hydroxide; lead(II) nitrate; camphor-10-sulfonic acid; dihydrogen peroxide; sodium acetate; dinitrogen tetraoxide; In tetrahydrofuran; dichloromethane; chloroform; acetone; 1: Ring cleavage / 2: Condensation / 3: Nitrosation / 4: Oxidation;
DOI:10.1139/v00-012

Reference yield:

: 294867-60-0
(1S,2R)-(-)-cis-1-phthalimido-2-O-acetylo-2-indanol

: 214139-27-2
BEA₃₈₈

Guidance literature:: Multi-step reaction with 2 steps

1: 65 percent / NaOMe / methanol; CH₂Cl₂ / 5 h / pH 7.5

With sodium methylate; In methanol; dichloromethane; 1: Deacetylation;
DOI:10.1139/v00-012