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Benzenesulfonamide, N-[3,5-bis(1-methylethyl)-4-oxo-2,5-cyclohexadien-1-ylidene]-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75531-77-0

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75531-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75531-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75531-77:
(7*7)+(6*5)+(5*5)+(4*3)+(3*1)+(2*7)+(1*7)=140
140 % 10 = 0
So 75531-77-0 is a valid CAS Registry Number.

75531-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,5-Diisopropyl-4-oxo-cyclohexa-2,5-dienylidene)-4-methyl-benzenesulfonamide

1.2 Other means of identification

Product number -
Other names -

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:75531-77-0 SDS

75531-77-0Relevant academic research and scientific papers

Synthesis and 13C NMR spectra of N-substituted p-quinonimines: III. N-arylthio- and N-arylsulfonyl-1,4-benzoquinonimines with enhanced electron-donor character of quinoid ring

Pirozhenko,Avdeenko,Yusina,Konovalova

, p. 1121 - 1128 (2007/10/03)

Incorporation of alkyl substituents into quinonimine fragments of N-arylthio- and N-arylsulfonyl-1,4-benzoquinonimines results in virtually equal changes in the chemical shifts of the carbon atoms from this fragment compared to those of unsubstituted and

EFFECT OF ARENESULFONAMIDE GROUP ON THE NATURE OF SUBSTITUTION IN THE AROMATIC RING. IV. REACTION OF DERIVATIVES OF 4-SULFONAMIDOPHENOL AND 1,4-DI(SULFONAMIDO)BENZENE WITH NITROSATING AGENTS

Zakatov, V.V.,Dubina, V.L.,Torubarnov, I.V.

, p. 303 - 306 (2007/10/02)

The action of nitrosating agents on derivatives of 4-sulfonamidophenol and 1,4-di(sulfonamido)benzene leads to the formation of either the nitration products or the oxidation products.

NATURE OF THE EFFECT OT THE SUBSTITUENT AT THE NITROGEN ATOM ON THE OXIDATION-REDUCTION POTENTIALS OF p-BENZOQUINONE MONOIMINES

Burmistrov, K. S.,Burmistrov, S. I.

, p. 1279 - 1284 (2007/10/02)

A series of N-acyl-substituted p-benzoquinone monoimines were synthesized.Their oxidation-reduction potentials were investigated, and were correlated with the ? constants and pKa values of the corresponding substituted benzoic acids.A conclusio

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