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Methyl N-Boc-4-hydroxypiperidine-3-carboxylate is a chemical compound with the molecular formula C13H21NO5. It is an ester derivative of N-Boc-4-hydroxypiperidine-3-carboxylic acid, characterized by its versatile structure and reactivity in organic synthesis and pharmaceutical research.

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  • 406212-51-9 Structure
  • Basic information

    1. Product Name: Methyl N-Boc-4-hydroxypiperidine-3-carboxylate
    2. Synonyms: Methyl N-Boc-4-hydroxypiperidine-3-carboxylate;1-tert-Butyl 3-Methyl 4-hydroxy-1,3-piperidinedicarboxylate;1,3-Piperidinedicarboxylic acid, 4-hydroxy-, 1-(1,1-diMethylethyl) 3-Methyl ester;1-tert-butyl 3-Methyl 4-hydroxypiperidine-1,3-dicarboxylate;4-Hydroxy-1,3-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 3-methyl ester;Methyl N-(tert-Butoxycarbonyl)-4-hydroxypiperidine-3-carboxylate
    3. CAS NO:406212-51-9
    4. Molecular Formula: C12H21NO5
    5. Molecular Weight: 259.29884
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 406212-51-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 352.1±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.182±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 14.12±0.40(Predicted)
    10. CAS DataBase Reference: Methyl N-Boc-4-hydroxypiperidine-3-carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl N-Boc-4-hydroxypiperidine-3-carboxylate(406212-51-9)
    12. EPA Substance Registry System: Methyl N-Boc-4-hydroxypiperidine-3-carboxylate(406212-51-9)
  • 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: 406212-51-9(Hazardous Substances Data)

406212-51-9 Usage

Uses

Used in Organic Synthesis:
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate is used as a building block for the synthesis of various biologically active molecules and pharmaceuticals. Its unique structure allows for the creation of a wide range of compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Methyl N-Boc-4-hydroxypiperidine-3-carboxylate is used as a reagent in the synthesis of diverse N-Boc-4-hydroxypiperidine-3-carboxylic acid derivatives. These derivatives have potential applications in drug discovery and development, making this compound a valuable chemical intermediate for the creation of new therapeutic agents.
Used in Drug Discovery and Development:
Methyl N-Boc-4-hydroxypiperidine-3-carboxylate is utilized in the development of new drugs, particularly those targeting specific biological pathways or diseases. Its versatility and reactivity make it an essential component in the design and synthesis of novel pharmaceutical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 406212-51-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,2,1 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 406212-51:
(8*4)+(7*0)+(6*6)+(5*2)+(4*1)+(3*2)+(2*5)+(1*1)=99
99 % 10 = 9
So 406212-51-9 is a valid CAS Registry Number.

406212-51-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-tert-butyl 3-O-methyl 4-hydroxypiperidine-1,3-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1-tert-butyl 3-methyl 4-hydroxy-1,3-piperidinedicarboxylate

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:406212-51-9 SDS

406212-51-9Downstream Products

406212-51-9Relevant articles and documents

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

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Paragraph 0212; 0213, (2014/05/08)

Provided are pyridopyrazine compounds of formula (1), pharmaceutical compositions thereof and methods of use therefore, wherein R1, R2, R3, R4 and m are as defined in the specification.

SUBSTITUTED PYRIDOPYRAZINES AS NOVEL SYK INHIBITORS

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Page/Page column 45, (2013/02/27)

Provided are certain pyridopyrazine compounds, pharmaceutical compositions thereof and methods of use therefor.

Pyridine derivatives

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, (2008/06/13)

Pyridine compounds of general formula: wherein —R1represents in which R11is hydrogen, C1-6alkyl, halogen, hydroxy, C1-12alkoxy, nitro, amino, C1-6alkylsulfonylamino, C1-6alkoxycarbonyl, C1-6alkylamino, di(C1-6alkyl)amino, C1-6alkanoylamino, phenyl C1-6alkylamino, phenylsulfonylamino, or —O—(CH2)n—R111; R2represents hydrogen or halogen; R3represents hydrogen, —CR31R32R33, or —NR34R35; R4is hydrogen, carbamoyl, CN, carboxyl, etc.; R5is amino, C1-6alkylamino, di C1-6alkylamino, etc. or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological activity.

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