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(3R,6S)-6-phenyl-5-(p-toluenesulfonyl)-3,6-dihydro-2H-pyran-3-yl N-benzyl carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

729593-90-2

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729593-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 729593-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,9,5,9 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 729593-90:
(8*7)+(7*2)+(6*9)+(5*5)+(4*9)+(3*3)+(2*9)+(1*0)=212
212 % 10 = 2
So 729593-90-2 is a valid CAS Registry Number.

729593-90-2Downstream Products

729593-90-2Relevant academic research and scientific papers

Base-induced enantioselective synthesis of sulfinyl dihydropyrans

Fernandez De La Pradilla, Roberto,Tortosa, Mariola

, p. 1217 - 1222 (2007/10/03)

2-Sulfinyl dienols undergo an efficient base-promoted cyclization to produce sulfinyl dihydropyrans with creation of two asymmetric centers. The configurational stability of the allylic sulfoxide in most cases is noteworthy. Simple manipulations lead to a

Sulfoxide-directed enantioselective synthesis of functionalized dihydropyrans

Fernaendez de la Pradilla, Roberto,Tortosa, Mariola

, p. 2157 - 2160 (2007/10/03)

The highly selective base-promoted cyclization of enantiopure sulfinyl dienols affords allylic sulfinyl dihydropyrans.

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