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TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE is a chemical compound that belongs to the class of piperidine derivatives. It is a carbamate derivative with a tert-butyl group attached to the piperidine ring, featuring an acetyl(methyl)amino group and a phenyl group. TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE may hold potential pharmaceutical applications, although further research is necessary to elucidate its properties and possible uses.

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  • TERT-BUTYL (4-(N-METHYLACETAMIDO)-4-PHENYLPIPERIDIN-1-YL)CARBAMATE

    Cas No: 182621-53-0

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  • 182621-53-0 Structure
  • Basic information

    1. Product Name: TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE
    2. Synonyms: TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE;1-Piperidinecarboxylic acid, 4-(acetylMethylaMino)-4-phenyl-, 1,1-diMethylethyl ester;4-[Acetyl(Methyl)aMino]-1-(Boc-aMino)-4-phenylpiperidine, 97%
    3. CAS NO:182621-53-0
    4. Molecular Formula: C19H28N2O3
    5. Molecular Weight: 332.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 182621-53-0.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: 1.548
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE(182621-53-0)
    11. EPA Substance Registry System: TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE(182621-53-0)
  • 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: 182621-53-0(Hazardous Substances Data)

182621-53-0 Usage

Uses

As the provided materials do not specify the exact applications of TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE, the following uses are hypothetical and based on the general properties of similar compounds:
Used in Pharmaceutical Industry:
TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE could be used as a pharmaceutical agent for [specific medical condition or therapeutic area] due to its unique chemical structure and potential interaction with biological targets.
Used in Chemical Research:
In the field of chemical research, TERT-BUTYL 4-[ACETYL(METHYL)AMINO]-4-PHENYLPIPERIDINE-1-CARBAMATE may serve as a research compound for studying the effects of its structural components on biological systems or for developing new synthetic pathways.

Check Digit Verification of cas no

The CAS Registry Mumber 182621-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,6,2 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182621-53:
(8*1)+(7*8)+(6*2)+(5*6)+(4*2)+(3*1)+(2*5)+(1*3)=130
130 % 10 = 0
So 182621-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H28N2O3/c1-15(22)20(5)19(16-9-7-6-8-10-16)11-13-21(14-12-19)17(23)24-18(2,3)4/h6-10H,11-14H2,1-5H3

182621-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[acetyl(methyl)amino]-4-phenylpiperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:182621-53-0 SDS

182621-53-0Relevant articles and documents

A reliable and efficient synthesis of SR 142801

Giardina,Grugni, Mario,Rigolio, Roberto,Vassallo, Marco,Erhard, Karl,Farina, Carlo

, p. 2307 - 2310 (2007/10/03)

A convenient synthesis of the potent human NK-3 receptor antagonist SR 142801, (S)-(+)-N-{{3-[1-benzoyl-3-(3,4-dichlorophenyl)piperidin-3-yl]prop-1 -yl}-4-phenylpiperidin-4-yl}-N-methylacetamide [(S)-(+)-(15)], is described. Improvements over the previously reported procedure are the preparation of the intermediate 5 via the novel imide 3 and subsequent reaction with the nucleophile 14, which reacts, regioselectively, at the endocyclic nitrogen.

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