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622-82-2

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622-82-2 Usage

Physical State

Liquid

Color

Colorless to pale yellow

Odor

Faint

Primary Use

Research and laboratory settings (chemical intermediate)

Secondary Use

Synthesis of other organic compounds

Hazardous Nature

Toxic

Potential Health Risks

Skin and eye irritation, harmful effects from long-term exposure

Safety Precautions

Follow proper safety protocols, use appropriate protective equipment to minimize risk of exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 622-82-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 622-82:
(5*6)+(4*2)+(3*2)+(2*8)+(1*2)=62
62 % 10 = 2
So 622-82-2 is a valid CAS Registry Number.

622-82-2SDS

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-ethyl-2-phenylhydrazine

1.2 Other means of identification

Product number -
Other names Hydrazine, 1-ethyl-2-phenyl-

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:622-82-2 SDS

622-82-2Relevant articles and documents

Aryl Pyrazoles from Photocatalytic Cycloadditions of Arenediazonium

Cardinale, Luana,Neumeier, Michael,Majek, Michal,Jacobi Von Wangelin, Axel

, p. 7219 - 7224 (2020/10/02)

A photocatalytic synthesis of 1,5-diaryl pyrazoles from arenediazoniums and arylcyclopropanols is reported. The reaction proceeded under mild conditions (rt, 20 min) with catalytic [Ru(bpy)3]2+ under blue-light irradiation and exhibited compatibility with several functional groups (e.g., I, SF5, SO2NH2, N3, CN) and perfect levels of regiocontrol. Mechanistic studies (luminescence spectroscopy, CV, DFT, radical trapping, quantum yield determination) documented an initial oxidative quenching of the excited photocatalyst and the operation of a radical-chain mechanism.

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