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(3aR,4S,7R,7aS)-2-(4-chlorophenyl)-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89104-84-7

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89104-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89104-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,0 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89104-84:
(7*8)+(6*9)+(5*1)+(4*0)+(3*4)+(2*8)+(1*4)=147
147 % 10 = 7
So 89104-84-7 is a valid CAS Registry Number.

89104-84-7Downstream Products

89104-84-7Relevant academic research and scientific papers

Target Specific Tactics in Olefin Metathesis: Synthetic Approach to cis-syn-cis-Triquinanes and -Propellanes

Kotha, Sambasivarao,Aswar, Vikas R.

, p. 1808 - 1811 (2016)

A concise and simple synthetic approach to cis-syn-cis-triquinanes and -propellanes has been demonstrated via olefin metathesis starting with exo-nadic anhydride. This approach involves a ring-opening and ring-closing metathesis sequence of norbornene derivatives using Grubb's catalyst. Early-stage diallylation of norbornene derivatives is demonstrated followed by ring-closing metathesis that delivers propellanes exclusively. Surprisingly, ring-opening metathesis, late-stage diallylation, followed by ring-closing metathesis delivers triquinane as well as propellane derivatives.

Mechanochemical Grinding Diels-Alder Reaction: Highly Efficient and Rapid Access to Bi-, Tri-, and Tetracyclic Systems

Agarwal, Jyoti,Rani, Rashmi,Peddinti, Rama Krishna

, p. 1336 - 1340 (2017/06/27)

Grinding of various electron-deficient dienophiles with diverse dienes in a pestle and mortar for 1-15 minutes afforded the corresponding Diels-Alder adducts in quantitative yields under catalyst-free and solvent-free conditions, without the necessity for

Synthesis and antidepressant-like action of stereoisomers of imidobenzenesulfonylaziridines in mice evaluated in the forced swimming test

Duarte, Filipe S.,Andrade, Evilazio da S.,Vieira, Ricardo A.,Uieara, Marina,Nunes, Ricardo J.,de Lima, Thereza C.M.

, p. 5397 - 5401 (2008/02/07)

The present study describes the chemical synthesis and pharmacological evaluation of a new series of eleven compounds stereoisomers of imidobenzenesulfonylaziridines in the forced-swimming test (FST) in mice. The pharmacological results of these compounds

Synthesis and characterization of exo-endo and endo-endo benzenesulfonylaziridines

Da Silva Andrade, Evilazio,Nunes, Ricardo Jose,Uieara, Marina

, p. 3073 - 3081 (2007/10/03)

In the search for structural cyclic imide analogues of therapeutic interest, the synthesis, separation, and characterization of exo-endo 3 and endo-endo 4 stereoisomers of benzenesulfonylaziridines, not found in the literature, are described in this study

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