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587-78-0

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587-78-0 Usage

Type of compound

Salt

Constituents

Pyridinium cation and bromide anion

Structural feature

4-fluorophenylmethyl group attached to the pyridinium ring

Application

Organic synthesis and pharmaceutical research

Role

Chiral ligand in asymmetric catalysis

Potential medical applications

Treatment of neurological disorders and cancer

Versatility

Range of potential uses in chemical and biomedical research

Check Digit Verification of cas no

The CAS Registry Mumber 587-78-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,8 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 587-78:
(5*5)+(4*8)+(3*7)+(2*7)+(1*8)=100
100 % 10 = 0
So 587-78-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11FN.BrH/c13-12-6-4-11(5-7-12)10-14-8-2-1-3-9-14;/h1-9H,10H2;1H/q+1;/p-1

587-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-fluorophenyl)methyl]pyridin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names -

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:587-78-0 SDS

587-78-0Relevant articles and documents

Coupling Photocatalysis and Substitution Chemistry to Expand and Normalize Redox-Active Halides

Rathnayake, Manjula D.,Weaver, Jimmie D.

supporting information, p. 2036 - 2041 (2021/04/05)

Photocatalysis can generate radicals in a controlled fashion and has become an important synthetic strategy. However, limitations due to the reducibility of alkyl halides prevent their broader implementation. Herein we explore the use of nucleophiles that can substitute the halide and serve as an electron capture motif that normalize the variable redox potentials across substrates. When used with photocatalysis, bench-stable, commercially available collidinium salts prove to be excellent radical precursors with a broad scope.

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