CAS 3105-95-1

Ácido L-pipecólico

Descripción:

Ácido L-pipecólico es un aminoácido cíclico caracterizado por su estructura de anillo de piperidina de seis miembros, que contiene un grupo funcional de ácido carboxílico. Es un compuesto que ocurre de forma natural, a menudo encontrado en varios sistemas biológicos, y juega un papel en el metabolismo de la lisina. La fórmula molecular de Ácido L-pipecólico es C6H11NO2, lo que indica la presencia de átomos de carbono, hidrógeno, nitrógeno y oxígeno. Este compuesto es típicamente un sólido cristalino blanco a blanco sucio y es soluble en agua, reflejando su naturaleza polar debido al grupo de ácido carboxílico. Ácido L-pipecólico es conocido por su participación en varias vías bioquímicas, incluyendo su posible papel como molécula de señalización y en la síntesis de otros compuestos bioactivos. Además, ha despertado interés en la investigación farmacéutica por sus posibles aplicaciones terapéuticas, particularmente en el contexto de trastornos neurológicos. Sus propiedades, como el punto de fusión y la reactividad específica, pueden variar según las condiciones ambientales y la pureza.

Fórmula: C₆H₁₁NO₂

InChI: InChI=1S/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)/t5-/m0/s1

Clave InChI: InChIKey=HXEACLLIILLPRG-YFKPBYRVSA-N

SMILES: C(O)(=O)[C@@H]1CCCCN1

Sinónimos:

• (-)-Pipecolic acid
• (-)-Pipecolinic acid
• (2S)-2-Piperidinecarboxylic acid
• (2S)-Piperidin-1-ium-2-carboxylate
• (2S)-piperidine-2-carboxylate
• (2S)-piperidine-2-carboxylic acid
• (S)-(-)-2-Piperidinecarboxylic Acid
• (S)-(-)-Pipecolic acid
• (S)-Pipecolinic acid
• (S)-Piperidine-2-carboxylic acid
• 2-Piperidinecarboxylic acid (2S)-
• 2-Piperidinecarboxylic acid, (S)-
• <span class="text-smallcaps">L</span>-(-)-Pipecolic acid
• <span class="text-smallcaps">L</span>-Homoproline
• <span class="text-smallcaps">L</span>-Pipecolinic acid
• <span class="text-smallcaps">L</span>-Piperidine-2-carboxylic acid
• L(-)-2-Pipecolinic acid
• L(-)-Pipecolinic Acid
• L-Homoproline
• NSC 93089

L-Pipecolic Acid

CAS: 3105-95-1

Fórmula: C₆H₁₁NO₂

Pureza: >98.0%(T)(HPLC)

Forma y color: White to Light yellow powder to crystal

Peso molecular: 129.16

Ref: 3B-P1404

L-Pipecolinic acid, 99%

CAS: 3105-95-1

L-Pipecolinic acid is involved in synaptic transmission in the central nervous system. It is also used as pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the leg

Fórmula: C₆H₁₁NO₂

Pureza: 99%

Forma y color: White to cream, Powder

Peso molecular: 129.16

Ref: 02-L15373

H-Homopro-OH

CAS: 3105-95-1

High enantioselectivies could be achieved (> 98% ee) when choosing L-pipecolic acid as catalyst for asymmetric Mannich reactions.

Fórmula: C₆H₁₁NO₂

Pureza: > 99%

Forma y color: Whitish

Peso molecular: 129.16

Ref: 01-4006540

2-Piperidinecarboxylic acid, (2S)-

CAS: 3105-95-1

Fórmula: C₆H₁₁NO₂

Pureza: 97%

Forma y color: Solid

Peso molecular: 129.1570

Ref: IN-DA00320V

L-Pipecolic acid

CAS: 3105-95-1

L-Pipecolic acid

Pureza: ≥98%

Peso molecular: 129.16g/mol

Ref: 54-BUP15882

L-Pipecolic acid

CAS: 3105-95-1

Fórmula: C₆H₁₁NO₂

Forma y color: White to off-white powder

Peso molecular: 129.16

Ref: 7W-GM6970

(L)-Pipecolinic acid

CAS: 3105-95-1

(L)-Pipecolinic acid

Fórmula: C₆H₁₁NO₂

Pureza: 98%

Forma y color: pale yellow solid

Peso molecular: 129.15703g/mol

Ref: 54-OR480636

L-Pipecolic acid

CAS: 3105-95-1

L-Pipecolic acid, a lysine metabolite, builds up in infants with peroxisomal genetic disorders like Zellweger syndrome.

Fórmula: C₆H₁₁NO₂

Pureza: 99.75%

Forma y color: Solid

Peso molecular: 129.16

Ref: TM-T4762

L-Pipecolic Acid

CAS: 3105-95-1

Applications Pipecolic acid is involved in synaptic transmission in the central nervous system. The l-form occurs in plants.
References Nomura Y., et al.: Neurochem. Res., 6, 391 (1981),

Fórmula: C₆H₁₁NO₂

Forma y color: Neat

Peso molecular: 129.16

Ref: TR-P479750

Pipecolic acid

CAS: 3105-95-1

Pipecolic acid is a metabolite of tryptophan that has been shown to inhibit the proliferation of pluripotent cells in vitro. Pipecolic acid was also shown to have a significant effect on the reaction mechanism of dinucleotide phosphate, which is essential for the synthesis of DNA and RNA. Pipecolic acid can be synthesized from picolinic acid through an amide bond formation. This compound is also found in wild-type strains as well as cancerous and infectious strains of bacteria. Pipecolic acid inhibits bacterial growth by binding to the active site of specific enzymes, such as methionine adenosyltransferase and ribonucleotide reductase, leading to the inhibition of protein synthesis and cell division. It has been shown to inhibit leukemia inhibitory factor (LIF) activity in vitro, suggesting that it may be involved in urinary infections.
Pipecolic acid can also be prepared using preparative high-performance liquid chromatography (prepar

Fórmula: C₆H₁₁NO₂

Pureza: Min. 95%

Forma y color: White Powder

Peso molecular: 129.16 g/mol

Ref: 3D-FP15563

L-(-)-Pipecolinic acid

CAS: 3105-95-1

Fórmula: C₆H₁₁NO₂

Pureza: 97%

Forma y color: Solid

Peso molecular: 129.159

Ref: 10-F040065