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(4S,6R)-6-Benzyloxymethyl-4-methyl-tetrahydro-pyran-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130129-15-6

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130129-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130129-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,2 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130129-15:
(8*1)+(7*3)+(6*0)+(5*1)+(4*2)+(3*9)+(2*1)+(1*5)=76
76 % 10 = 6
So 130129-15-6 is a valid CAS Registry Number.

130129-15-6Relevant articles and documents

Hydroxyl-directed cyclopropanation of Z-allylsilanes

Mohr, Peter

, p. 7221 - 7224 (1995)

Z-5-Hydroxy-alk-2-enyl-silanes of general structure 1 are cyclopropanated by an excess of CH2l2 / Et2Zn in good yield and excellent stereoselectivity. Ensuing protodesilylation, however, lacks efficient regiocontrol and affords syn-products 5 in modest yield but high stereochemical purity.

New asymmetric synthesis of a pheromone component of the shield bug Cantao Parentum

Mineeva

, p. 398 - 405 (2014/06/09)

A novel procedure has been developed for the synthesis of (2S,4R,6R,8S)-2,4,8-trimethyl-1,7-dioxaspiro[5.5]undecane, a pheromone component of the shield bug Cantao Parentum, through intermediate cyclopropanol derivatives in the key stages of carbon chain

A CONVERGENT ENANTIOCONTROLLED ROUTE TO MEVALONOLACTONE AND VITAMIN E FROM (S)-O-BENZYLGLYCIDOL

Takano, Seiichi,Shimazaki, Youichi,Iwabuchi, Yoshiharu,Ogasawara, Kunio

, p. 3619 - 3622 (2007/10/02)

A convergent enantiocontrolled route to (+) and (-)-mevalonolactones and vitamin E has been developed using (S)-O-benzylglycidol as the sole chiral block.

Enantio-and Stereo-controlled Construction of Tertiary and Quaternary Carbon Centers Using Chiral O-Benzylglycidol as Template

Takano, Seiichi,Shimazaki, Youichi,Moriya, Minoru,Ogasawara, Kunio

, p. 1177 - 1180 (2007/10/02)

An efficient method for the enantio- and stereo-controlled construction of tertiary and quaternary carbon centers in a highly functionalized system has been developed using chiral O-benzylglycidol as template.

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