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1-Naphthalenemethanol, decahydro-2-hydroxy-5,5,8a-trimethyl-, a-(4-methylbenzenesulfonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59633-92-0

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59633-92-0 Usage

Type of compound

Synthetic organic compound

Use

Chiral auxiliary in organic synthesis

Application

Asymmetric synthesis to control the stereochemistry of reactions

Classification

Sulfonate ester

Derivation

Derived from 1-naphthalenemethanol

Contains

Sulfonic acid group

Group

Methylbenzenesulfonate group

Benefits

Easy purification and isolation of the compound

Industries

Pharmaceutical and agrochemical

Purpose

Synthesis of complex organic molecules with specific stereochemical configurations

Check Digit Verification of cas no

The CAS Registry Mumber 59633-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,3 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59633-92:
(7*5)+(6*9)+(5*6)+(4*3)+(3*3)+(2*9)+(1*2)=160
160 % 10 = 0
So 59633-92-0 is a valid CAS Registry Number.

59633-92-0Relevant academic research and scientific papers

Lewis Acid and Photochemically Mediated Cyclization of Olefinic β-Keto Esters

White, James D.,Skeean, Richard W.,Trammell, Gary L.

, p. 1939 - 1948 (2007/10/02)

Olefinic β-keto esters 8, 17, and 20, prepared by either carbomethoxylation of the parent ketone or alkylation of the dianion of methyl acetoacetate with the allylic bromide, underwent cyclization with stannic chloride in dichloromethane to give mono- and

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