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Benzenepropanoic acid, α-(hydroxymethyl)-, ethyl ester, (R)-, also known as (R)-α-Hydroxymethylbenzenepropanoic acid ethyl ester, is a chiral organic compound with the molecular formula C12H16O3. It is a derivative of benzenepropanoic acid, featuring a hydroxymethyl group (-CH2OH) at the α-position and an ethyl ester group (-COOCH2CH3) at the carboxylic acid end. Benzenepropanoic acid, a-(hydroxymethyl)-, ethyl ester, (R)- is a racemic mixture, with the (R)-enantiomer being one of the two possible stereoisomers. It is used in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of chiral compounds. The compound's structure and properties make it a valuable building block in the development of new drugs and other chemical products.

87884-40-0

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87884-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87884-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87884-40:
(7*8)+(6*7)+(5*8)+(4*8)+(3*4)+(2*4)+(1*0)=190
190 % 10 = 0
So 87884-40-0 is a valid CAS Registry Number.

87884-40-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (RS)-tropic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 2-(hydroxymethyl)-3-phenylpropionate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:87884-40-0 SDS

87884-40-0Downstream Products

87884-40-0Relevant academic research and scientific papers

PROCESS FOR PRODUCING OPTICALLY ACTIVE 3-HYDROXYPROPIONIC ESTER DERIVATIVE

-

Page/Page column 12, (2010/02/13)

The present invention is to provide a process for simply producing an optically active 3-hydroxypropionic ester derivative useful as a medicament intermediate from an inexpensive material. More specifically, the present invention is directed to a process for producing an optically active 3-hydroxypropionic ester derivative comprising reacting an acetic ester derivative available at low cost with a base and a formic ester, thereby converting the acetic ester derivative into a 2-formylacetic ester derivative, and thereafter, stereospecifically reducing the formyl group of the derivative by use of an enzymatic source capable of stereoselectively reducing the formyl group of the derivative.

Stereochemical Studies. LX. Neighboring Phenyl Group Participation. I. Stereospecific Transformation of L-Phenylalanine to Optically Active Tropic Acid

Juang, Tzuoh Miin,Yamada, Shun-ichi

, p. 4426 - 4430 (2007/10/02)

Trifluoroacetolysis of (S)-3-phenyllactic acid ester sulfonate((S)-7), obtained from L-phenylalanine via nitrous acid deamination followed by ethanolysis, afforded (R)-tropic acid ester((R)-8) in good yield by phenyl migration with inversion, while acetol

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