39834-40-7

Basic information

• Product Name: (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL
• Synonyms: (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL;Trans-2-Bromo-1-TeTralol
• CAS NO: 39834-40-7
• Molecular Formula: C₁₀H₁₁BrO
• Molecular Weight: 227.09774
• Mol File: 39834-40-7.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 337°C at 760 mmHg
• Flash Point: 157.6°C
• Appearance: /
• Density: 1.538g/cm³
• Vapor Pressure: 4.23E-05mmHg at 25°C
• Refractive Index: 1.628
• CAS DataBase Reference: (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(39834-40-7)
• EPA Substance Registry System: (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL(39834-40-7)

Safety Data

• Hazardous Substances Data: 39834-40-7(Hazardous Substances Data)

Usage

General Description

(1S,2R)-2-Bromo-1,2,3,4-tetrahydro-naphthalen-1-ol is a chemical compound with the molecular formula C10H13BrO. It is a chiral compound that contains a bromine atom and a hydroxyl group attached to a tetrahydro-naphthalene ring. (1S,2R)-2-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-OL is used in organic synthesis and medicinal chemistry as a building block for the preparation of various biologically active compounds. It can also be utilized as a precursor for the synthesis of pharmaceuticals and agrochemicals. Additionally, it may have potential applications in the field of fragrance and flavoring due to its aromatic nature.

InChI:InChI=1/C10H11BrO/c11-9-6-5-7-3-1-2-4-8(7)10(9)12/h1-4,9-10,12H,5-6H2/t9-,10+/m1/s1

Upstream product

• 119-64-2 tetralin 
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• 447-53-0 1,2-Dihydronaphthalene 
• 75238-77-6 1-Bromo-1,2,3,4-tetrahydronaphthalene 
• 529-33-9 1,2,3,4-Tetrahydro-1-naphthol 
• 91-20-3 naphthalene 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 2018-87-3 1,2-dibromo-1,2,3,4-tetrahydro-naphthalene 

Downstream Products

• 127531-61-7 trans-1-(2-hydroxyethylcyclohexylamino)-1,2,3,4-tetrahydro-2-naphthol 
• 155932-36-8 indan-1-carbaldehyde 
• 109470-12-4 trans-1-Benzoylamino-2-hydroxy-tetralin 
• 112108-01-7 ecopipam 
• 91-59-8 naphthalen-2-ylamine 
• 32338-05-9 2-(phenylsulfonyl)naphthalene 
• 7570-96-9 2-naphthyl phenyl sulfide 
• 7570-98-1 1-naphthyl phenyl sulfide 
• 20937-86-4 2-azidonaphthalene 
• 6921-40-0 1-azidonaphthalene 

Relevant articles and documents

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Oxidative β-Halogenation of Alcohols: A Concise and Diastereoselective Approach to Halohydrins

β-Halohydrins bearing transformable halo- and hydroxyl groups, are easily converted into various valuable blocks in organic and pharmaceutical synthesis. A diastereoselective β-halogenation of benzylic alcohols was achieved under simple and low-cost conditions, which provided a direct synthesis of β-halohydrins. The simple reaction conditions, easily available reagents, high diastereoselectivities, and additional oxidant-free make this reaction very attractive and practical.

From simple organobromides or olefins to highly value-added bromohydrins: A versatile performance of dimethyl sulfoxide

A novel and efficient direct transformation of secondary bromides or olefins to highly value-added bromohydrins has been disclosed. Dimethyl sulfoxide (DMSO), a cheap and common solvent, performs its versatile role as a solvent, an essential oxidant, and also as an oxygen source in this bromohydrin synthesis.