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Benzenesulfonic acid, 4-[4-[[4-(dimethylamino) phenyl]methylene]-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl]-, sodium salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63044-60-0

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63044-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63044-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,4 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63044-60:
(7*6)+(6*3)+(5*0)+(4*4)+(3*4)+(2*6)+(1*0)=100
100 % 10 = 0
So 63044-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H19N3O4S.Na/c1-13-18(12-14-4-6-15(7-5-14)21(2)3)19(23)22(20-13)16-8-10-17(11-9-16)27(24,25)26;/h4-12H,1-3H3,(H,24,25,26);/q;+1/p-1/b18-12-;

63044-60-0SDS

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 sodium,4-[(4Z)-4-[[4-(dimethylamino)phenyl]methylidene]-3-methyl-5-oxopyrazol-1-yl]benzenesulfonate

1.2 Other means of identification

Product number -
Other names Benzenesulfonic acid,4-(4-((4-(dimethylamino)phenyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)-,sodium salt (1:1)

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:63044-60-0 SDS

63044-60-0Downstream Products

63044-60-0Relevant academic research and scientific papers

Photoinduced Decomposition of Arene Diazonium Salts by Pyrazolone and Naphthole Dyes

Timpe, H.-J.,Schubert, E.,Worschech, S.

, p. 955 - 963 (2007/10/02)

The pyrazolone dyes 1-4 in their photoexcited singlet states bleached out by arene diazonium salts which dediazoniate during the reaction.Both compounds react in equal proportion.The quantum yields increase with the increasing of the concentration and electron acceptor properties of the diazonium salts and increasing of the electron donor properties of the dyes.The quantum yields of dye bleaching decrease on addition of DABCO or allylic thiourea, whereas the dediazoniation is not influenced.A kinetic model based on a primary electron transfer from the excited dye to arene diazonium salt is presented and used to determine rate constants for individual partial reactions.

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