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77275-11-7

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77275-11-7 Usage

Molecular structure

Contains a styryl group (C=C-CH=CH2) attached to a pyridine ring

Reactivity

High reactivity

Applications

Building block in organic synthesis, pharmaceutical research, material science research, synthesis of complex organic molecules, fluorescent probe, and component in organic light-emitting diodes (OLEDs)

Family

Styrylpyridine

Versatility

Wide range of potential applications in academic research and industrial processes

Check Digit Verification of cas no

The CAS Registry Mumber 77275-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77275-11:
(7*7)+(6*7)+(5*2)+(4*7)+(3*5)+(2*1)+(1*1)=147
147 % 10 = 7
So 77275-11-7 is a valid CAS Registry Number.

77275-11-7SDS

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 2-[(E)-2-(2-methylphenyl)ethenyl]pyridine

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:77275-11-7 SDS

77275-11-7Downstream Products

77275-11-7Relevant articles and documents

Br?nsted acid-catalysed conjugate addition of photochemically generated α-amino radicals to alkenylpyridines

Hepburn, Hamish B.,Melchiorre, Paolo

supporting information, p. 3520 - 3523 (2016/03/04)

The conjugate addition of α-amino radicals to alkenylpyridines has been accomplished by the synergistic merger of Br?nsted acid and visible light photoredox catalysis. Key to reaction development was the protonation of the alkenylpyridines that transientl

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