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(1R,2S,4S,4'S)-1,3,3-trimethyl-4'-phenylspiro[bicyclo[2.2.1]heptane-2,2'-[1,3]oxathiolane] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1311140-47-2

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1311140-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1311140-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,1,4 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1311140-47:
(9*1)+(8*3)+(7*1)+(6*1)+(5*1)+(4*4)+(3*0)+(2*4)+(1*7)=82
82 % 10 = 2
So 1311140-47-2 is a valid CAS Registry Number.

1311140-47-2Downstream Products

1311140-47-2Relevant academic research and scientific papers

Reaction of optically active oxiranes with thiofenchone and 1-methylpyrrolidine-2-thione: Formation of 1,3-oxathiolanes and thiiranes

Fu, Changchun,Linden, Anthony,Heimgartner, Heinz

, p. 773 - 784 (2011)

The SnCl4-catalyzed reaction of (-)-thiofenchone (=1,3,3-trimethylbicyclo[2.2.1]heptane-2-thione; 10) with (R)-2-phenyloxirane ((R)-11) in anhydrous CH2Cl2 at -60° led to two spirocyclic, stereoisomeric 4-phenyl-1,3-oxathiolanes 12 and 13 via a regioselective ring enlargement, in accordance with previously reported reactions of oxiranes with thioketones (Scheme 3). The structure and configuration of the major isomer 12 were determined by X-ray crystallography. On the other hand, the reaction of 1-methylpyrrolidine-2-thione (14a) with (R)-11 yielded stereoselectively (S)-2-phenylthiirane ((S)-15) in 56% yield and 87-93% ee, together with 1-methylpyrrolidin-2-one (14b). This transformation occurs via an SN2-type attack of the S-atom at C(2) of the aryl-substituted oxirane and, therefore, with inversion of the configuration (Scheme 4). The analogous reaction of 14a with (R)-2-{[(triphenylmethyl)oxy] methyl}oxirane ((R)-16b) led to the corresponding (R)-configured thiirane (R)-17b (Scheme 5); its structure and configuration were also determined by X-ray crystallography. A mechanism via initial ring opening by attack at C(3) of the alkyl-substituted oxirane, with retention of the configuration, and subsequent decomposition of the formed 1,3-oxathiolane with inversion of the configuration is proposed (Scheme 5). Copyright

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