(R)-1,2,3,4-tetrahydronaphthalen-2-ol

Base Information

• Chemical Name: (R)-1,2,3,4-tetrahydronaphthalen-2-ol
• CAS No.: 7575-89-5
• Molecular Formula: C₁₀H₁₂O
• Molecular Weight: 148.205
• DSSTox Substance ID: DTXSID70348789
• Nikkaji Number: J593.029D
• Wikidata: Q82123757

Synonyms:7575-89-5;(R)-1,2,3,4-tetrahydronaphthalen-2-ol;2-Naphthalenol, 1,2,3,4-tetrahydro-, (2R)-;(2R)-1,2,3,4-tetrahydronaphthalen-2-ol;(r)-beta-tetralol;Tetralin-2alpha-ol;starbld0010180;SCHEMBL6951241;DTXSID70348789;AKOS037651949

Chemical Property of (R)-1,2,3,4-tetrahydronaphthalen-2-ol

Chemical Property:

• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 148.088815002
• Heavy Atom Count: 11
• Complexity: 133

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CC2=CC=CC=C2CC1O
• Isomeric SMILES: C1CC2=CC=CC=C2C[C@@H]1O

Technology Process of (R)-1,2,3,4-tetrahydronaphthalen-2-ol

There total 43 articles about (R)-1,2,3,4-tetrahydronaphthalen-2-ol 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: 96.0%

1,2,3,4-tetrahydronaphthalen-2-one (530-93-8) → (S)-2-tetralol (530-91-6,7575-89-5,113725-16-9,20107-40-8)

Guidance literature:

With formic acid; C₂₉H₃₈N₃O₂RuS; triethylamine; at 40 ℃; for 15h; Reagent/catalyst; enantioselective reaction; Inert atmosphere;

DOI:10.1002/adsc.201500288

Reference yield: 93.0%

(1R,2S)-1,2,3,4-tetrahydronaphthalene-1,2-diol (57495-92-8) → (S)-2-tetralol (530-91-6,7575-89-5,113725-16-9,20107-40-8)

Guidance literature:

With hydrogen; acetic acid; palladium on activated charcoal; In ethyl acetate;

DOI:10.1016/S0957-4166(02)00098-8

Reference yield: 25.0%

vinyl acetate (108-05-4,9003-20-7) + 1,2,3,4-tetrahydronaphthalen-2 ol (530-91-6) → (S)-2-tetralol (530-91-6,7575-89-5,113725-16-9,20107-40-8) + (S)-1,2,3,4-tetrahydronaphthalen-2-yl acetate (71601-10-0)

Guidance literature:

With 50 U aminoacylase E_.C_. 3.5.1.14; In hexane; for 168h;

DOI:10.1016/S0957-4166(00)00118-X

upstream raw materials:

1,2-naphthaquinone 1-<(2S,3S)-1,4-dimethoxy-2,3-butylene>acetal

1,2,3,4-tetrahydronaphthalen-2-one

2R-2-hydroxyl (2H)-naphthalenone (2S,3S)-1,4-dimethoxy-2,3-butylene acetal

(R)-(Indanylcarbinyl-1)-p-toluolsulfonat

Downstream raw materials:

(2R)-2-amino-1,2,3,4-tetrahydronaphthalene

(S)-((S)-1,2,3,4-tetrahydronaphthalen-2-yl) 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate

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