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Benzenesulfonamide, N-[[(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl]sulfinyl]-, (1R)- is a complex organic compound with the chemical formula C15H23NO2S. It is a derivative of benzenesulfonamide, featuring a sulfinyl group attached to the nitrogen atom. The compound has a chiral center at the carbon atom adjacent to the sulfinyl group, with the (1R)- configuration indicating the specific arrangement of atoms in the molecule. Benzenesulfonamide, N-[[(6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl]sulfinyl]-, (1R)- is characterized by its bicyclic structure, with two methyl groups attached to the bridgehead carbon atoms of the bicyclo[3.1.1]heptane ring. It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.

88195-46-4

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88195-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88195-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88195-46:
(7*8)+(6*8)+(5*1)+(4*9)+(3*5)+(2*4)+(1*6)=174
174 % 10 = 4
So 88195-46-4 is a valid CAS Registry Number.

88195-46-4Relevant academic research and scientific papers

Regiospecific Two-Step Synthesis of Optically Active Allylic Terpenyl Thiols

Gadras, A.,Dunogues, J.,Calas, R.,Deleris, G.

, p. 442 - 444 (2007/10/02)

Allylic thiols were prepared in 70-90 percent yields by treatment of mono- and sesquiterpenes with C6H5SO2N=S=O followed by LiAlH4 reduction of the ene adducts.

ALKYLATION DE TERPENES EN DEUX ETAPES PAR ENE-REACTION

Deleris, G.,Dunogues, J.,Gadras, A.

, p. 2135 - 2138 (2007/10/02)

A simple, two-step homologation of terpenes is reported that requires ene-reaction with PhSO2NSO and subsequent of the intermediate adducts with CuI catalyzed Grignard

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