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1823-44-5

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1823-44-5 Usage

Uses

2-(2-Thiazolylazo)-p-cresol is a heterocyclic azo-dye2, has been used:as iron binding ligand during determination of iron speciation in seawater by cathodic stripping voltammetryin spectrophotometric determination of vanadium, titanium, lead, indium and nickelas as a spectrophotometric reagent in the determination of uranium in mine drainage water samples

Check Digit Verification of cas no

The CAS Registry Mumber 1823-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1823-44:
(6*1)+(5*8)+(4*2)+(3*3)+(2*4)+(1*4)=75
75 % 10 = 5
So 1823-44-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H9N3OS/c1-7-2-3-9(14)8(6-7)12-13-10-11-4-5-15-10/h2-6H,1H3,(H,11,13)/b12-8+

1823-44-5 Well-known Company Product Price

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  • Aldrich

  • (294543)  2-(2-Thiazolylazo)-p-cresol  97%

  • 1823-44-5

  • 294543-1G

  • 600.21CNY

  • Detail

1823-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-THIAZOLYLAZO)-P-CRESOL

1.2 Other means of identification

Product number -
Other names 4-methyl-2-thiazol-2-ylazo-phenol

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:1823-44-5 SDS

1823-44-5Upstream product

1823-44-5Relevant articles and documents

Catalytic oxidation of hydrazo derivatives promoted by a TiCl 3/HBr system

Drug, Eyal,Gozin, Michael

, p. 13784 - 13785 (2008/04/11)

Through a novel catalytic process of general synthetic interest, hydrazo compounds were efficiently and selectively converted into corresponding azo derivatives. The proposed mechanism of this process comprises two separate and distinctive catalytic cycle

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