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1622-15-7

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1622-15-7 Usage

Type of compound

Formazan dye

Common use

Redox indicator in biological and chemical research

Color

Bright red

Property

High molar absorptivity

Application

Spectrophotometric analysis of reducing agents

Fields of application

Biochemistry, pharmacology, and toxicology

Purpose

Measuring cell viability and assessing cytotoxicity of substances

Known for

Stability and low toxicity

Value

Valuable tool in scientific research

Check Digit Verification of cas no

The CAS Registry Mumber 1622-15-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1622-15:
(6*1)+(5*6)+(4*2)+(3*2)+(2*1)+(1*5)=57
57 % 10 = 7
So 1622-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H15ClN4/c20-16-13-11-15(12-14-16)19(23-21-17-7-3-1-4-8-17)24-22-18-9-5-2-6-10-18/h1-14,21H/b23-19-,24-22+

1622-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-anilino-4-chloro-N-phenyliminobenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names C-p-Chlorphenyl-N-phenyl-N'-phenylformazan

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:1622-15-7 SDS

1622-15-7Relevant articles and documents

Triphenyl verdazyl radicals' reactivity with alkyne carboxylates as a synthetic route to 1-(phenyldiazenyl)isoquinoline-3,4-dicarboxylates

Bancerz, Matthew,Prack, Ernest,Georges, Michael K.

supporting information; experimental part, p. 4026 - 4029 (2012/08/13)

A series of 1-(phenyldiazenyl)isoquinoline-3,4-dicarboxylates are synthesized by a unique reaction of triphenyl verdazyl radical with di-substituted electron deficient alkyne carboxylates. This transformation allows for the quick synthesis of this class of compounds in just three steps starting from a hydrazone. A radical mechanism that is consistent for the substitution patterns observed in the series of compounds made is proposed. The final product is obtained by a subsequent retro-Diels-Alder reaction.

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