59234-40-1

Basic information

• Product Name: CIS-2,6-PIPERIDINE DICARBOXYLIC ACID
• Synonyms: CIS-2,6-PIPERIDINE DICARBOXYLIC ACID
• CAS NO: 59234-40-1
• Molecular Formula: C₇H₁₁NO₄
• Molecular Weight: 173.17
• Mol File: 59234-40-1.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: CIS-2,6-PIPERIDINE DICARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: CIS-2,6-PIPERIDINE DICARBOXYLIC ACID(59234-40-1)
• EPA Substance Registry System: CIS-2,6-PIPERIDINE DICARBOXYLIC ACID(59234-40-1)

Safety Data

• Hazardous Substances Data: 59234-40-1(Hazardous Substances Data)

Upstream product

• 499-83-2 Pyridine-2,6-dicarboxylic acid 
• 922-54-3 2,6-diaminopimelic acid 
• 99669-83-7 trans-2,6-piperidinedicarboxamide 
• 59234-40-1 cis-meso-piperidine-2,6-dicarboxylic acid 
• 14289-34-0 (S,S)-2,6-diaminopimelic acid 
• 583-93-7 (2R,6R)-2,6-diaminoheptanedioic acid 
• 99669-83-7 meso-piperidine-2,6-dicarboxamide 

Downstream Products

• 499-82-1 (+/-)-trans-piperidine-2,6-dicarboxylic acid 
• 59234-48-9 dimethyl meso-(2R,6S)-piperidine-2,6-dicarboxylate hydrochloride 

Relevant articles and documents

Stereo-selective preparation of teneraic acid, trans-(2S,6S)-piperidine-2,6-dicarboxylic acid, via anodic oxidation and cobalt-catalyzed carbonylation

Teneraic acid (piperidine-2,6-dicarboxylic acid) is a naturally occurring imino acid that comprises three stereoisomers due to its two asymmetric centers at C2 and C6. The configuration of natural teneraic acid is reported to correspond to trans-(2S,6S).

Synthesis and evaluation of novel macrocyclic and acyclic ligands as contrast enhancement agents for magnetic resonance imaging

Novel chelates PIP-DTPA, AZEP-DTPA, NETA, NPTA, and PIP-DOTA were synthesized and evaluated as potential magnetic resonance imaging (MRI) contrast enhancement agents. The T1 and T2 relaxivities of their corresponding Gd(III) complexe

Synthesis of a key intermediate in the diaminopimelate pathway to L-lysine: 2,3,4,5-tetrahydrodipicolinic acid

2,3,4,5-Tetrahydrodipicolinic acid (3) is a key intermediate in the diaminopimelate (DAP) pathway to L-lysine (7). It was synthesized as the stable racemic potassium salt (25) from dipicolinic acid (14) by esterification, hydrogenation to the cis-diester (17), followed by elimination of p-toluenesulfinic acid from the N-toluenesulfonyl derivative (24) of dimethyl cis-piperidine-2,6-dicarboxylate with concomitant cleavage of the esther groups. (±)-2,3,4,5-Tetrahydrodipicolinic acid is unstable in neutral or acidic solution, and in basic solution it exists in equilibrium with the corresponding enamine (27) and 2-oxo-6-aminoadipate (26).