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236406-33-0

Tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate is a chemical compound with the molecular formula C14H27NO3. It is a derivative of piperidine, featuring a tert-butyl group, a hydroxyethyl group, and a methyl group. tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate is often utilized in pharmaceutical research and drug development due to its potential as a therapeutic agent. Its molecular structure and functional groups may confer biological activity, making it a candidate for the treatment of various medical conditions. Furthermore, it can serve as a building block for synthesizing other organic compounds with biological or pharmacological applications.

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  • 236406-33-0 Structure

  • Basic information

    1. Product Name: tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate
    2. Synonyms: tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate
    3. CAS NO:236406-33-0
    4. Molecular Formula: C13H25NO3
    5. Molecular Weight: 243
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 236406-33-0.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.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate(236406-33-0)
    11. EPA Substance Registry System: tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate(236406-33-0)

  • 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: 236406-33-0(Hazardous Substances Data)

236406-33-0 Usage

Uses

Used in Pharmaceutical Research and Drug Development:
Tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate is used as a potential therapeutic agent in pharmaceutical research and drug development for its possible biological activity. Its unique molecular structure and functional groups may contribute to its efficacy in treating various medical conditions.
Used in the Synthesis of Organic Compounds:
In the field of organic chemistry, tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate is used as a building block for the synthesis of other organic compounds. Its versatile structure allows for the creation of new compounds with potential biological or pharmacological applications, expanding the scope of chemical and medicinal research.

Check Digit Verification of cas no

The CAS Registry Mumber 236406-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,6,4,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 236406-33:
(8*2)+(7*3)+(6*6)+(5*4)+(4*0)+(3*6)+(2*3)+(1*3)=120
120 % 10 = 0
So 236406-33-0 is a valid CAS Registry Number.

236406-33-0SDS

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 tert-butyl 4-(2-hydroxyethyl)-4-methylpiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names N-t-butoxycarbonyl-4-methylpiperidine-4-ethanol

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:236406-33-0 SDS

236406-33-0Relevant articles and documents

NOVEL PIPERIDINE/8-AZABICYCLO [3.2.1] OCTAN DERIVATIVES AS MODUILATORS OF CHEMOKINE RECEPTOR CCR5

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Page/Page column 73, (2010/02/15)

Compounds of formula (I) wherein neither R4 nor R5 is hydrogen; compositions comprising them, processes for preparing them and their use in medical therapy (for example modulating CCR5 receptor activity in a warm blooded animal).

N-acyl cyclic amine derivatives

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, (2008/06/13)

The invention relates to compounds represented by the general formula [I][wherein Ar means an aryl group or a heteroaryl group which may have a substitutive group selected from a group consisting of a halogen atom, a lower alkyl group and a lower alkoxy group; R1 means a C3-C6 cycloalkyl group which is substitutable with a fluorine atom; R2 and R4 mean hydrogen atoms, groups represented by -(A1)m-NH-B or the like; R3 and R5 mean hydrogen atoms, C1-C6 aliphatic hydrocarbon groups or the like which are substitutable with a lower alkyl group(s); n means 0 or 1; and X means an oxygen atom or a sulfur atom]. Compounds according to the invention, since they not only have potent selective antagonistic activity against muscarinic M3 receptors but also exhibit excellent oral activity, durability of action and pharmacokinetics, are very useful as safe and effective remedies against respiratory, urinary and digestive diseases with little adverse side effects.

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