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6-FLUORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85072-31-7

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85072-31-7 Usage

Molecular structure

composed of a naphthalene ring with a fluorine atom attached to the 6th carbon and a hydroxyl group attached to the 2nd carbon

Physical properties

colorless or pale yellow liquid at room temperature

Biological properties

acts as a potent inhibitor of cytochrome P450 enzymes

Applications

used in various industrial and research applications, studied for potential use in the synthesis of pharmaceuticals and agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 85072-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,7 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85072-31:
(7*8)+(6*5)+(5*0)+(4*7)+(3*2)+(2*3)+(1*1)=127
127 % 10 = 7
So 85072-31-7 is a valid CAS Registry Number.

85072-31-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-1,2,3,4-tetrahydronaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 6-FLUORO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-OL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85072-31-7 SDS

85072-31-7Upstream product

85072-31-7Downstream Products

85072-31-7Relevant academic research and scientific papers

Gold-catalyzed oxidative coupling reactions with aryltrimethylsilanes

Brenzovich Jr., William E.,Brazeau, Jean-Francois,Toste, F. Dean

supporting information; experimental part, p. 4728 - 4731 (2010/12/25)

During continuing studies with a novel oxidative gold oxyarylation reaction, arylsilanes were found to be competent coupling partners, providing further evidence for an intramolecular electrophilic aromatic substitution mechanism. While providing yields complementary to those of the previously described boronic acid methods, the use of trimethylsilanes reduces the observation of homocoupling byproducts and allows for facile intramolecular coupling reactions.

Herbicidal bicyclic compounds

-

, (2008/06/13)

This invention relates to certain bicyclic derivatives which are indane and tetralin compounds and which have herbicidal properties, to processes for their preparation, to herbicidal compositions containing them and to a method of using them as herbicides

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