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bis-[(1S,2R,3S,5R)-2-(tert-butyl-dimethyl-silanyloxymethyl)-6,6-dimethyl-bicyclo[3.1.1]hept-3-yl] disulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

858658-58-9

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858658-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858658-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,6,5 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 858658-58:
(8*8)+(7*5)+(6*8)+(5*6)+(4*5)+(3*8)+(2*5)+(1*8)=239
239 % 10 = 9
So 858658-58-9 is a valid CAS Registry Number.

858658-58-9Relevant academic research and scientific papers

Enantioselective synthesis of either enantiomer of α-alkyl-α- hydroxy-α-phenylacetic acids using chiral auxiliaries

Perez-Estrada, Salvador,Lagunas-Rivera, Selene,Vargas-Diaz, Maria Elena,Velazquez-Ponce, Pedro,Joseph-Nathan, Pedro,Zepeda, L. Gerardo

, p. 1837 - 1843 (2005)

The enantioselective synthesis of either enantiomer of α-alkyl- α-hydroxy-α-phenylacetic acids was achieved by using 2-acyloxathianes 1a-c and the mixed acyl-S,O-acetals 7 and 8 as chiral auxiliaries, which can straightforwardly be prepared from (1R)-(-)-myrtenal. This procedure allowed the preparation of the title compounds in >95% enantiomeric excess (ee).

New S,O-acetals from (1R)-(-)-myrtenal as chiral auxiliaries in nucleophilic additions

Chacón-García, Luis,Lagunas-Rivera, Selene,Pérez-Estrada, Salvador,Vargas-Díaz, M. Elena,Joseph-Nathan, Pedro,Tamariz, Joaquín,Zepeda, L. Gerardo

, p. 2141 - 2145 (2007/10/03)

Treatment of hydroxythiol 4 with α,α-diethoxyacetophenone at room temperature yielded a mixture of epimeric S,O-acetals 6 and 7 (1:4, 92% yield), which were efficiently separated by flash chromatography. The OTBS derivatives 8 and 9 were treated with several Grignard reagents to afford carbinols 10 and 13 respectively (85-99% yield, >95% dr). After successive hydrolysis and reduction of 10 and 13 it is possible to obtain either enantiomer of diols 16 in high optical purity (>95% er).

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