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1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-[(phenylsulfonyl)oxy]- is a complex organic compound with the molecular formula C15H13NO4S. It is a derivative of isoindole, a heterocyclic aromatic compound, and features a tetrahydro structure with a phenylsulfonyl group attached to the 2-position. 1H-Isoindole-1,3(2H)-dione, 3a,4,7,7a-tetrahydro-2-[(phenylsulfonyl)oxy]- is characterized by its unique chemical structure, which includes a fused ring system and a sulfonyl ether functional group. It is likely to be found in research settings, particularly in the fields of organic chemistry and medicinal chemistry, where it may be studied for its potential applications or properties. The compound's specific uses and properties would depend on its reactivity, stability, and interaction with other molecules, which are not detailed in this summary.

87813-96-5

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87813-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87813-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,1 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87813-96:
(7*8)+(6*7)+(5*8)+(4*1)+(3*3)+(2*9)+(1*6)=175
175 % 10 = 5
So 87813-96-5 is a valid CAS Registry Number.

87813-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzenesulfonyloxy-(3ar,7ac)-3a,4,7,7a-tetrahydro-isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-Benzolsulfonyloxy-(3ar,7ac)-3a,4,7,7a-tetrahydro-isoindol-1,3-dion

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

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More Details:87813-96-5 SDS

87813-96-5Relevant academic research and scientific papers

Imides: Part IV - Synthesis and Reactions of N-(Arylsulphonyloxy)cyclohex-4-ene-1,2-dicarboximides

Aly, N. F.,El-Komy, M.,Aly, N. Y.,Orabi, M. O. A.

, p. 471 - 476 (2007/10/02)

N-(Arylsulphonyloxy)cyclohex-4-ene-1,2-dicarboximides (IIa and IIb) undergo base-catalysed Lossen rearrangement with aromatic amines in refluxing ethanol to give mixtures of N-(2-arylcarbamoyl)cyclohex-4-enyl-N'-arylureas (IIIa-d) and the amine salts of arylsulphonic acids (IVa-h).Fusion of II with aromatic amines for 15 min gives mixtures of 3-arylquinazoline-2,4-diones (VIa-c) and IV; however fusion for 1 hr affords mixtures of sym-N,N'-diarylureas (VIIa-d) and IV.Compounds IIa and IIb also react with phenylhydrazine to give mixtures of VIII and phenylhydrazine saltof arylsulphonic acids (IXa and IXb).The mass spectra of IIb and IIIa are presented, and discussed.

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