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(R)-1-(2-Hydroxymethyl-phenyl)-ethanol is a chiral chemical compound with the molecular formula C9H12O2. It is known for its two enantiomeric forms, with the (R)-enantiomer being the focus of this description. (R)-1-(2-Hydroxymethyl-phenyl)-ethanol is characterized by the presence of a hydroxyl group and a phenyl group, which contribute to its versatility in organic synthesis.

136113-11-6

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136113-11-6 Usage

Uses

Used in Pharmaceutical Industry:
(R)-1-(2-Hydroxymethyl-phenyl)-ethanol is used as a building block for the synthesis of various pharmaceutical compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Fragrance Industry:
In the fragrance industry, (R)-1-(2-Hydroxymethyl-phenyl)-ethanol serves as an intermediate for the development of new scents. Its chemical properties make it suitable for use in creating complex and diverse fragrances.
Used in Drug Development:
(R)-1-(2-Hydroxymethyl-phenyl)-ethanol has been identified for its biological activity, making it a promising candidate for drug development. Its potential applications in medicinal chemistry are currently being explored to develop new treatments for various health conditions.
Used in Medicinal Chemistry:
As a versatile intermediate, (R)-1-(2-Hydroxymethyl-phenyl)-ethanol is utilized in medicinal chemistry for the synthesis of compounds with potential therapeutic benefits. Its unique structure and functional groups enable the development of novel molecules for use in the treatment of various diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 136113-11-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,1 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136113-11:
(8*1)+(7*3)+(6*6)+(5*1)+(4*1)+(3*3)+(2*1)+(1*1)=86
86 % 10 = 6
So 136113-11-6 is a valid CAS Registry Number.

136113-11-6Upstream product

136113-11-6Downstream Products

136113-11-6Relevant academic research and scientific papers

A New Approach to Remote Asymmetric Induction in the Diastereoselective Reduction of γ-Keto Esters by Use of a Chiral Podand as Chiral Auxiliary

Tamai, Yasufumi,Koike, Shinji,Ogura, Atsuhiko,Miyano, Sotaro

, p. 799 - 800 (1991)

An efficient 1,7-asymmetric induction was achieved with up to 82percent diastereoisomeric excess (d.e.) in the diastereoselective reduction of the γ-keto ester 4 and o-acetylbenzoate 6 using a chiral podand 2 as a chiral auxiliary.

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