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Methanetricarboxylic acid, [(1R)-2,3-dihydro-1H-inden-1-yl]-, triethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

666824-82-4

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666824-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 666824-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,6,8,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 666824-82:
(8*6)+(7*6)+(6*6)+(5*8)+(4*2)+(3*4)+(2*8)+(1*2)=204
204 % 10 = 4
So 666824-82-4 is a valid CAS Registry Number.

666824-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl (1R)-2,3-dihydro-1H-inden-1-ylmethanetricarboxylate

1.2 Other means of identification

Product number -
Other names 2-Ethoxycarbonyl-2-(R)-indan-1-yl-malonic acid diethyl ester

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:666824-82-4 SDS

666824-82-4Downstream Products

666824-82-4Relevant academic research and scientific papers

Stereoselective carbon-carbon bond forming reactions between various chiral alkyl aryl carbinols and triethyl methanetricarboxylate by oxidation-reduction condensation using alkyl diphenylphosphinites

Mukaiyama, Teruaki,Nagata, Yuzo,Ikegai, Kazuhiro

, p. 1676 - 1677 (2007/10/03)

Oxidation-reduction condensation reactions between alkyl diphenylphosphinites derived from chiral alkyl aryl carbinols and triethyl methanetricarboxylate proceeded smoothly to afford the corresponding condensation products in good yields with inversion of stereochemistries. Copyright

Stereoselective Carbon-Carbon Bond Formation via the Mitsunobu Displacement of Chiral Secondary Benzylic Alcohols

Hillier, Michael C.,Desrosiers, Jean-Nicolas,Marcoux, Jean-Francois,Grabowski, Edward J. J.

, p. 573 - 576 (2007/10/03)

(Matrix presented) The stereoselective displacement of a variety of chiral benzylic alcohols with triethylmethanetricarboxylate (TEMT) under Mitsunobu conditions (DEAD, PMe3) has been demonstrated to proceed in good yield (70-94%) and with a high degree of inversion. Subsequent saponification and decarboxylation of the products thus obtained provide chiral 3-aryl-3-substituted propanoic acids without racemization.

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