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126150-99-0

3-Piperidinecarboxylicacid,4-hydroxy-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126150-99-0 Structure

  • Basic information

    1. Product Name: 3-Piperidinecarboxylicacid,4-hydroxy-(9CI)
    2. Synonyms: 3-Piperidinecarboxylicacid,4-hydroxy-(9CI);4-hydroxy-3-Piperidinecarboxylic acid
    3. CAS NO:126150-99-0
    4. Molecular Formula: C6H11NO3
    5. Molecular Weight: 145.15644
    6. EINECS: N/A
    7. Product Categories: CARBOXYLICACID
    8. Mol File: 126150-99-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Piperidinecarboxylicacid,4-hydroxy-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Piperidinecarboxylicacid,4-hydroxy-(9CI)(126150-99-0)
    11. EPA Substance Registry System: 3-Piperidinecarboxylicacid,4-hydroxy-(9CI)(126150-99-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 126150-99-0(Hazardous Substances Data)

126150-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126150-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126150-99:
(8*1)+(7*2)+(6*6)+(5*1)+(4*5)+(3*0)+(2*9)+(1*9)=110
110 % 10 = 0
So 126150-99-0 is a valid CAS Registry Number.

126150-99-0Downstream Products

126150-99-0Relevant articles and documents

Hydroxy- and amino-substituted piperidinecarboxylic acids as γ-aminobutyric acid agonists and uptake inhibitors

Jacobsen,Labouta,Schaumburg,Falch,Krogsgaard-Larsen

, p. 1157 - 1162 (2007/10/02)

The syntheses of (3RS, 4RS)-4-hydroxypiperidine-3-carboxylic acid (4), (3RS, 5SRJ-5-hydroxypiperiden-3-carboxylic acid (20), (3RS, 4SR)-4-acetamidopiperidine-3-carboxylic acid (10), and (3RS, 5SR)-5-acetamidopiperidine-3-carboxylic acid (18), related to the specific γ-aminobutyric (GABA) uptake inhibitors (RS)-piperidine-3-carboxylic acid (nipecotic acid) and (3RS, 4SR)-4-hydroxypiperidine-3-carboxylic acid (21), are described. Furthermore, (3RS, 4SR)-3-hydroxypiperidine-4-carboxylic acid (14), related to the specific GABA agonist piperidine-4-carboxylic acid (isonipecotic acid), has been synthesized. The structures of 4, 10, 14, 18, and 20 have been established by 270-MHz 1H NMR spectroscopic analyses. The affinity of the compounds for the GABA receptors and for the neuronal (synaptosomal) GABA uptake system in vitro has been measured. Compound 14 interacts selectively with the GABA receptors but less effectively than isonipecotic acid and the cis-isomer 22. Compounds 4, 18, and 20 are inhibitors of the GABA uptake system, although much weaker than nipecotic acid and (3RS, 4SR)-4-hydroxypiperidine-3-carboxylic acid (21). Compound 10 is inactive in both test systems.

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