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182621-53-0

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182621-53-0 Usage

General Description

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. The compound also contains an acetyl(methyl)amino group and a phenyl group. This chemical may have potential pharmaceutical applications, but further research is required to fully understand its properties and potential uses.

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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