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824431-19-8

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824431-19-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 824431-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,4,3 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 824431-19:
(8*8)+(7*2)+(6*4)+(5*4)+(4*3)+(3*1)+(2*1)+(1*9)=148
148 % 10 = 8
So 824431-19-8 is a valid CAS Registry Number.

824431-19-8SDS

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-[bis[(1,5-dimethylpyrazol-3-yl)methyl]amino]ethanol

1.2 Other means of identification

Product number -
Other names Ethanol,2-[bis[(1,5-dimethyl-1H-pyrazol-3-yl)methyl]amino]

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:824431-19-8 SDS

824431-19-8Downstream Products

824431-19-8Relevant articles and documents

Synthesis and enzyme inhibitory activities of some new pyrazole-based heterocyclic compounds

Harit, Tariq,Malek, Fouad,Bali, Brahim El,Khan, Ajmal,Dalvandi, Kourosh,Marasini, Bishnu P.,Noreen, Shagufta,Malik, Rizwana,Choudhary, M. Iqbal,Khan, Sadia

, p. 2772 - 2778,7 (2012)

Three tridentate N,N-bis(3,5-dimethylpyrazol- 1-ylmethyl)-1-hydroxy-2- aminoethane (2), N,N-bis(3,5-dimethylpyrazol- 1-ylmethyl)-cyclohexylamine (3) and 2-[bis (1,5-dimethyl-1H-pyrazol-3-ylmethyl)amino]ethan-1-ol (4) are synthesized and spectroscopically characterized togetherwith 1-hydroxymethyl-3,5-dimethylpyrazole (1). These have been tested in inhibitory activities against various hyperactive enzymes like urease, β- glucuronidase, phosphodiesterase, α-chymotrypsin, acetylcholinesterase and butyrylcholinesterase. Compounds 1, 2 and 3 were found to be selective inhibitors of urease. Compound 4 was found to be selective inhibitor of butyrylcholinesterase. The nature of the junction between pyrazoles cycles determined the activities of these tripods. While the tripods are inactive towards urease or glucuronidase, they turn to be selective towards butyrylcholinesterase.

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