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85819-03-0

2,4-Piperidinedicarboxylic acid, also known as trans-1,2-Cyclohexanedicarboxylic acid, is a cyclic chemical compound with the molecular formula C7H11NO4. It is commonly used in the synthesis of pharmaceuticals and as a building block in organic chemistry due to its versatile properties.
Used in Pharmaceutical Industry:
2,4-Piperidinedicarboxylic acid is used as a key intermediate in the development of drugs for various purposes. It plays a crucial role in the formulation of medications targeting neurological disorders and has potential as a treatment for cocaine addiction.
Used as a Chiral Auxiliary:
In the field of asymmetric synthesis, 2,4-Piperidinedicarboxylic acid serves as a chiral auxiliary, aiding in the synthesis of enantiomerically pure compounds, which is essential for the production of many pharmaceuticals.
Used as a Ligand in Metal-Catalyzed Reactions:
2,4-Piperidinedicarboxylic acid is utilized as a ligand in metal-catalyzed reactions, enhancing the efficiency and selectivity of these processes, which is vital for the advancement of chemical synthesis techniques.
Overall, 2,4-Piperidinedicarboxylic acid is a valuable and versatile chemical with significant applications in both the pharmaceutical and chemical industries, contributing to the development of new drugs and innovative synthetic methods.

85819-03-0

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85819-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85819-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85819-03:
(7*8)+(6*5)+(5*8)+(4*1)+(3*9)+(2*0)+(1*3)=160
160 % 10 = 0
So 85819-03-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h4-5,8H,1-3H2,(H,9,10)(H,11,12)

85819-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name piperidine-2,4-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 2,4-Piperidinedicarboxylic acid

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:85819-03-0 SDS

85819-03-0Relevant articles and documents

Synthesis of (2S*,4R*,5S*)-piperidinetricarboxylic acid, a non-proteinogenic amino acid isolated from clitocybe acromelalga

Hashimoto, Kimiko,Higashibayashi, Shuhei,Shirahama, Haruhisa

, p. 581 - 588 (2007/10/03)

(255*,4R*,5S*)-Piperidinetricarboxylic acid isolated from a poisonous mushroom Clitocybe acromelalga was synthesized along with its stereoisomers and their depolarizing activity was tested.

SYNTHESIS AND CONFIGURATION OF DIASTEREOMERIC 2,4-, 2,5-, AND 2,6-PIPERIDINEDICARBOXYLIC ACIDS AND THEIR DIMETHYL ESTERS

Mastafanova, L. I.,Turchin, K. F.,Evstratova, M. I.,Sheinker, Yu. N.,Yakhontov, L. N.

, p. 305 - 309 (2007/10/02)

The reduction in an acidic medium over a platinum catalysts of 2,4-, 2,5-, and 2,6-pyridinedicarboxylic acids gave cis-2,4-, -2,5-, and -2,6-piperidinedicarboxylic acids, heating of which in an alkaline medium led to thermodynamically equilibrium mixtures of diastereomers.Individual trans-2,5-piperidinecarboxylic acid was isolated.The configurations of the 2,4-, 2,5-, and 2,6-piperidinedicarboxylic acids and their methyl esters were established by means of the PMR spectra.

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