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878572-03-3

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878572-03-3 Usage

Type of alcohol

Secondary alcohol

Functional groups

Hydroxyl (-OH) and phenyl (C6H5)

Substituents on phenyl group

Chlorine (Cl) and fluorine (F) atoms

Potential applications

Pharmaceutical and agrochemical industries

Use

Building block for the preparation of biologically active molecules

Relevance

Valuable tool for research in organic chemistry and related fields

Safety concerns

Health and environmental risks if not managed properly

Handling

Careful handling required due to potential risks

Check Digit Verification of cas no

The CAS Registry Mumber 878572-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,5,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 878572-03:
(8*8)+(7*7)+(6*8)+(5*5)+(4*7)+(3*2)+(2*0)+(1*3)=223
223 % 10 = 3
So 878572-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClFO/c1-5(11)6-2-3-8(10)7(9)4-6/h2-5,11H,1H3

878572-03-3SDS

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 1-(3-chloro-4-fluorophenyl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(3-chloro-4-fluorophenyl)ethan-1-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:878572-03-3 SDS

878572-03-3Downstream Products

878572-03-3Relevant articles and documents

Exploring Tandem Ruthenium-Catalyzed Hydrogen Transfer and SNAr Chemistry

Polidano, Kurt,Reed-Berendt, Benjamin G.,Basset, Ana?s,Watson, Andrew J. A.,Williams, Jonathan M. J.,Morrill, Louis C.

supporting information, p. 6716 - 6719 (2017/12/26)

A hydrogen-transfer strategy for the catalytic functionalization of benzylic alcohols via electronic arene activation, accessing a diverse range of bespoke diaryl ethers and aryl amines in excellent isolated yields (38 examples, 70% average yield), is reported. Taking advantage of the hydrogen-transfer approach, the oxidation level of the functionalized products can be selected by judicious choice of simple and inexpensive additives.

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