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2-Piperidinone, 3-hydroxy-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33341-99-0 Structure
  • Basic information

    1. Product Name: 2-Piperidinone, 3-hydroxy-1-methyl-
    2. Synonyms: 3-hydroxy-1-methyl-piperidin-2-one;1-methyl-2-oxo-3-piperidinol;1-Methyl-3-hydroxy-piperidon-2;3-hydroxy-1-methylpiperidin-2-one;
    3. CAS NO:33341-99-0
    4. Molecular Formula: C6H11NO2
    5. Molecular Weight: 129.15700
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33341-99-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Piperidinone, 3-hydroxy-1-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Piperidinone, 3-hydroxy-1-methyl-(33341-99-0)
    11. EPA Substance Registry System: 2-Piperidinone, 3-hydroxy-1-methyl-(33341-99-0)
  • 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: 33341-99-0(Hazardous Substances Data)

33341-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33341-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33341-99:
(7*3)+(6*3)+(5*3)+(4*4)+(3*1)+(2*9)+(1*9)=100
100 % 10 = 0
So 33341-99-0 is a valid CAS Registry Number.

33341-99-0Relevant articles and documents

Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones

Kamal, Ahmed,Ramana, K. Venkata,Ramana, A. Venkata,Babu, A. Hari

, p. 2587 - 2594 (2003)

The enantioselective synthesis of 3-hydroxypyrrolidin-2-ones and 3-hydroxy piperidin-2-ones has been carried out in high enantiomeric excess employing immobilized lipase from Pseudomonas cepacia.

SMALL MOLECULE INHIBITORS OF NF-kB INDUCING KINASE

-

, (2020/12/11)

The present invention relates to compounds that inhibit NIK and pharmaceutical compositions comprising such compounds and methods of using the same. These compounds and pharmaceutical compositions are envisaged to be useful for preventing or treating diseases such as cancer (such as B-cell malignancies including leukemias, lymphomas and myeloma), inflammatory disorders, autoimmune disorders, immunodermatologic disorders such as palmoplantar pustulosis and hidradenitis suppurativa, and metabolic disorders such as obesity and diabetes.

6,5-HETEROCYCLIC PROPARGYLIC ALCOHOL COMPOUNDS AND USES THEREFOR

-

, (2015/05/06)

The invention relates to novel compounds of Formula I: wherein A, Y, R1, R2 and the subscript b each has the meaning as described herein and compounds of Formula I, and stereoisomers, geometric isomers, tautomers, solvates, metabolites, isotopes, pharmaceutically acceptable salts, or prodrugs thereof. Compounds of Formula I and pharmaceutical compositions thereof are useful in the treatment of disease and disorders in which undesired or over-activation of NF-kB signaling is observed.

SYNTHESIS WITH HYDROXYLACTAMES III A FACILE ENTRY TO THE 1-OXO-β-CARBOLINE SKELETON. SYNTHESIS OF STRYCHNOCARPINE

Herdeis, Claus,Dimmerling, Anna

, p. 2277 - 2283 (2007/10/02)

Strychnocarpine 1c is synthesized via hydrogenation of 1-methyl-3-hydroxypyridone(2) with Ru/C.Fischer indole cyclization of phenylhydrazone 11 yields 1c.

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