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87327-65-9

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87327-65-9 Usage

Description

2,6-Difluoro-α-methylbenzenemethanol is an organic compound characterized by the presence of two fluorine atoms at the 2nd and 6th positions on a benzene ring, with an α-methylbenzyl alcohol group attached. This unique structure endows it with specific chemical properties that make it a valuable intermediate in the synthesis of various pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
2,6-Difluoro-α-methylbenzenemethanol is used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties. Its presence in the molecular structure of these pharmaceuticals can contribute to their therapeutic effects and pharmacological profiles, making it an essential component in the development of new drugs and medications.

Check Digit Verification of cas no

The CAS Registry Mumber 87327-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87327-65:
(7*8)+(6*7)+(5*3)+(4*2)+(3*7)+(2*6)+(1*5)=159
159 % 10 = 9
So 87327-65-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8F2O/c1-5(11)8-6(9)3-2-4-7(8)10/h2-5,11H,1H3

87327-65-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H32771)  1-(2,6-Difluorophenyl)ethanol, 97%   

  • 87327-65-9

  • 1g

  • 415.0CNY

  • Detail
  • Alfa Aesar

  • (H32771)  1-(2,6-Difluorophenyl)ethanol, 97%   

  • 87327-65-9

  • 10g

  • 2524.0CNY

  • Detail

87327-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,6-Difluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(2,6-difluorophenyl)ethanol

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:87327-65-9 SDS

87327-65-9Upstream product

87327-65-9Relevant articles and documents

COMPOUNDS, COMPOSITIONS, AND METHODS OF USE

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Paragraph 0345, (2020/12/11)

Described herein are compounds that act as CYP46A1 inhibitors, compositions comprising these compounds, and methods of their use into treating neurodegenerative diseases and the like, or a pharmaceutically active salt thereof. The present invention relates to compounds represented by the formula wherein each symbol is as defined in the specification, or a pharmaceutically active salt thereof.

Chemoselective reduction of the carbonyl functionality through hydrosilylation: Integrating click catalysis with hydrosilylation in one pot

Roy, Sudipta Raha,Sau, Samaresh Chandra,Mandal, Swadhin K.

, p. 9150 - 9160 (2014/12/11)

Herein we report the chemoselective reduction of the carbonyl functionality via hydrosilylation using a copper(I) catalyst bearing the abnormal N-heterocyclic carbene 1 with low (0.25 mol %) catalyst loading at ambient temperature in excellent yield within a very short reaction time. The hydrosilylation reaction of α,β-unsaturated carbonyl compounds takes place selectively toward 1,2-addition (C=O) to yield the corresponding allyl alcohols in good yields. Moreover, when two reducible functional groups such as imine and ketone groups are present in the same molecule, this catalyst selectively reduces the ketone functionality. Further, 1 was used in a consecutive fashion by combining the Huisgen cycloaddition and hydrosilylation reactions in one pot, yielding a range of functionalized triazole substituted alcohols in excellent yields.

ANTAGONISTS OF LYSOPHOSPHATIDIC ACID RECEPTORS

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Page/Page column 27, (2010/06/22)

Described herein are compounds that are antagonists of lysophosphatidic receptor(s). Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such antagonists, alone and in combination with other compounds, for treating LPA-dependent or LPA-mediated conditions or diseases.

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