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Pyridine, 4-(diazophenylmethyl)-, also known as 4-(phenylmethylidene)pyridine or 4-benzylidene-1-phenyl-1H-pyridin-1-ium, is an organic compound with the chemical formula C12H10N. It is a derivative of pyridine, featuring a diazophenylmethyl group attached to the 4-position of the pyridine ring. Pyridine, 4-(diazophenylmethyl)- is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is essential to handle Pyridine, 4-(diazophenylmethyl)- with care, following proper safety protocols.

832-82-6

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832-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 832-82-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 832-82:
(5*8)+(4*3)+(3*2)+(2*8)+(1*2)=76
76 % 10 = 6
So 832-82-6 is a valid CAS Registry Number.

832-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[diazo(phenyl)methyl]pyridine

1.2 Other means of identification

Product number -
Other names phenylpyridyldiazomethane

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:832-82-6 SDS

832-82-6Downstream Products

832-82-6Relevant academic research and scientific papers

Copper-Catalyzed Oxidation of Hydrazones to Diazo Compounds Using Oxygen as the Terminal Oxidant

Liu, Wenbin,Twilton, Jack,Wei, Bo,Lee, Maizie,Hopkins, Melissa N.,Bacsa, John,Stahl, Shannon S.,Davies, Huw M. L.

, p. 2676 - 2683 (2021/03/03)

A mild method for accessing diazo compounds via aerobic oxidation of hydrazones is described. This catalytic transformation employs a Cu(OAc)2/pyridine catalyst and molecular oxygen from ambient air as the terminal oxidant, generating water as the sole byproduct and affording the desired diazo compounds within minutes at room temperature. A broad array of electronically diverse aryldiazo esters, ketones, and amides can be accessed. Pyridine dramatically enhances the rate of the reaction by solubilizing the copper catalyst and serving as the Br?nsted base in the turnover-limiting proton-coupled oxidation of hydrazone by copper(II). Insights gained from mechanistic studies led to expansion of the scope of this method to include diaryl hydrazones, delivering diaryl diazomethane derivatives, which cannot be accessed via established diazo transfer methods. The products of this method may be employed in rhodium carbene catalysis without isolation of the diazo intermediate to afford cyclopropane products in good yield with high enantioselectivity.

SMALL MOLECULE LFA-1 INHIBITORS

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Page/Page column 124, (2016/01/01)

The present invention relates to novel compounds which are capable of inhibiting the interaction of LFA-1 with its counter ligands.

Substituted diaryldiazomethanes and diazofluorenes: Structure, reactivity and stability

Davis, Philip J.,Harris, Lawrence,Karim, Aman,Thompson, Amber L.,Gilpin, Martin,Moloney, Mark G.,Pound, Matthew J.,Thompson, Claire

supporting information; experimental part, p. 1553 - 1556 (2011/04/26)

The synthesis of several substituted diaryldiazomethanes and diazofluorenes, and an assessment of their structure, reactivity and stability, is reported.

+ HYDROGEN BOND IN ORGANIC RADICAL SOLID

Okuno, Tsunehisa,Otsuka, Takeo,Awaga, Kunio

, p. 57 - 64 (2007/10/03)

Reaction of m- or p-pyridyl nitronyl nitroxide (m- or p-PYNN) with HBr gas gave a 2:1 complex between them.The IR spectra of (m- and p-PYNN)2HBr indicates an intermolecular + hydrogen bond between two pyridyl rings. (m-PYNN)2HBr shows ferr

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