Welcome to LookChem.com Sign In|Join Free

CAS

  • or

499-82-1

Post Buying Request

499-82-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

499-82-1 Usage

General Description

2,6-piperidinedicarboxylic acid, also known as pipecolic acid, is a cyclic amino acid that is naturally found in the human body and in various plants. It plays an important role in the biosynthesis of the neurotransmitter gamma-aminobutyric acid (GABA), which is involved in regulating neuronal activity in the brain. Pipecolic acid has also been identified as a modulator of immune responses and inflammation. In addition, it has potential therapeutic applications in the treatment of neurological disorders, such as epilepsy and schizophrenia. Pipecolic acid is also used as a building block in the synthesis of pharmaceuticals and agrochemicals. Overall, 2,6-piperidinedicarboxylic acid has diverse biological activities and potential applications in medicine and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 499-82-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 499-82:
(5*4)+(4*9)+(3*9)+(2*8)+(1*2)=101
101 % 10 = 1
So 499-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO4/c9-6(10)4-2-1-3-5(8-4)7(11)12/h4-5,8H,1-3H2,(H,9,10)(H,11,12)

499-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Piperidine-2,6-dicarboxylic Acid

1.2 Other means of identification

Product number -
Other names Piperidin-2,6-dicarbonsaeure

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:499-82-1 SDS

499-82-1Downstream Products

499-82-1Relevant articles and documents

Photocatalytic stereoselective N-cyclization of 2,6-diaminopimelic acid into piperidine-2,6-dicarboxylic acid by an aqueous suspension of activated cadmium(II) sulfide particles

Ohtani, Bunsho,Kusakabe, Satoshi,Okada, Katsumi,Tsuru, Shigeto,Nishimoto, Sei-Ichi,Amino, Yusuke,Izawa, Kunisuke,Nakato, Yoshihiro,Matsumura, Michio,Nakaoka, Yasuhiro,Nosaka, Yoshio

, p. 201 - 209 (2007/10/03)

Photoirradiation at a wavelength of >300 nm of a deaerated suspension of cadmium(II) sulfide (CdS) particles in an aqueous solution of a mixture of stereoisomers of 2,6-diaminopimelic acid (DAP; (S,S):(R,S):(R,R) = 1:2:1) produced piperidine-2,6-dicarboxylic acid (PDC) via a redox-combined mechanism including oxidation and reduction by positive holes and photoexcited electrons, respectively. Both the yield and trans:cis ratio of PDC markedly depended on the kinds of CdS photocatalysts, their pre-treatment, and the loading of fine platinum (or its oxide) particles. A CdS photocatalyst prepared by heat treatment of a commercial powder in hexagonal (wurtzite) structure at 1023 K in the presence of a small amount of air gave the highest yield and trans:cis ratio. Analyses of the activated CdS powder by powder X-ray diffraction (XRD), photoluminescence (PL), X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), and BET surface area measurements revealed the formation of sulfur vacancies due to heat treatment, which promote the photoinduced cadmium metal (Cd0) deposition. The Cd0, deposited in situ on the CdS surface and detected by reduction of methylviologen, may act as a reduction site for photoexcited electrons toward a cyclic Schiff base intermediate produced by oxidation of DAP with positive holes followed by deamination and intramolecular condensation. Optically pure (R,R)- or (S,S)-PDCs were prepared successfully by photocatalytic reaction with the activated CdS particles using (R,R)- or (S,S)-DAPs, indicating that stereoselective conversion of organic compounds can be achieved via photocatalytic reaction under controlled conditions.

Improvement of photocatalytic activity and product selectivity by cadmium metal deposited in situ on suspended cadmium(II) sulfide particles

Ohtani, Bunsho,Kusakabe, Satoshi,Nishimoto, Sei-ichi,Matsumura, Michio,Nakato, Yoshihiro

, p. 803 - 804 (2007/10/03)

Effect of annealing of commercial crystalline CdS powders on their photocatalytic activity and product selectivity was investigated for stereoselective diamino-N-cyclization of 2,6-diaminopimelic acid operated in deaerated aqueous solution.Surface analyses revealed the formation of sulfur vacancy, which promotes the photoinduced cadmium metal (Cd0) deposition.The Cd0, detected by reduction of methylviologen, may act as reduction site for photoexcited electrons.

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 499-82-1