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(S)-3-[(S)-hydroxy(phenyl)methyl]-5,7-dimethoxy-3H-isobenzofuran-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1373919-81-3

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1373919-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1373919-81-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,9,1 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1373919-81:
(9*1)+(8*3)+(7*7)+(6*3)+(5*9)+(4*1)+(3*9)+(2*8)+(1*1)=193
193 % 10 = 3
So 1373919-81-3 is a valid CAS Registry Number.

1373919-81-3Upstream product

1373919-81-3Downstream Products

1373919-81-3Relevant articles and documents

CN-assisted oxidative cyclization of cyano cinnamates and styrene derivatives: A facile entry to 3-substituted chiral phthalides

Reddy, R.Santhosh,Kiran, I. N. Chaithanya,Sudalai, Arumugam

, p. 3655 - 3661 (2012)

The asymmetric dihydroxylation (AD) of o-cyano cinnamates and styrene derivatives leads to efficient construction of chiral phthalide frameworks in high optical purities. This unique reaction is characterized by unusual synergism between CN and osmate groups resulting in rate enhancement of the AD process. The method is amply demonstrated by the synthesis and the structural/stereochemical assignment of the natural products.

A SINGLE STEP ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF 3-SUBSTITUTED CHIRAL PHTHALIDES

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Page/Page column 17; 48; 49, (2013/06/05)

The present invention discloses single step, highly enantioselective catalytic oxidative cyclization process for the synthesis of 3-substituted chiral phthalides. In particular, the invention discloses asymmetric synthesis of chiral phthalides via synergetic nitrile accelerated oxidative cyclization of o-cyano substituted aryl alkenes in high yield and enantiomeric excess (ee) in short reaction time. Also, disclosed herein is "one -pot" asymmetric synthesis of biologically important natural compounds having 3-substituted chiral phthalide structural framework in the molecule.

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