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Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate is a complex organic chemical compound that features a piperidine ring with a Boc protecting group and an ethyl ester, along with a phenylethylamino substituent. Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate is characterized by its potential pharmaceutical applications, which may include acting as a central nervous system stimulant or serving as a precursor to other bioactive compounds. Its carboxylate ester nature also suggests it could function as a prodrug, converting into an active pharmaceutical agent within the body.

1016259-54-3

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1016259-54-3 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate is used as a precursor compound for the synthesis of other pharmacologically active substances. Its unique structure, including the Boc protecting group and the phenylethylamino substituent, makes it a candidate for further chemical modifications to enhance its biological activity.
Used in Research and Development:
In the field of medicinal chemistry, Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate is utilized as a research tool to explore its potential as a central nervous system stimulant. Its structure allows scientists to investigate its interactions with biological targets and evaluate its efficacy and safety in preclinical studies.
Used in Drug Design:
Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate is employed as a building block in the design of new drugs. Its carboxylate ester functionality suggests it could be developed into a prodrug, which would be converted into the active pharmaceutical ingredient after administration, potentially improving the drug's pharmacokinetic properties.
Further research and development are essential to fully understand the capabilities and limitations of Ethyl 1-Boc-3-(1-phenylethylaMino)piperidine-4-carboxylate, ensuring its safe and effective use in various applications within the pharmaceutical and medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1016259-54-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,6,2,5 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1016259-54:
(9*1)+(8*0)+(7*1)+(6*6)+(5*2)+(4*5)+(3*9)+(2*5)+(1*4)=123
123 % 10 = 3
So 1016259-54-3 is a valid CAS Registry Number.

1016259-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name O1-tert-butyl O4-ethyl 3-(1-phenylethylamino)piperidine-1,4-dicar boxylate

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

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More Details:1016259-54-3 SDS

1016259-54-3Downstream Products

1016259-54-3Relevant academic research and scientific papers

A novel asymmetric synthesis of cis-(3R,4R)-N-(tert -butoxycarbonyl)-4- methyl-3-(methylamino)piperidine

Hao, Bao-Yu,Liu, Jin-Qiang,Zhang, Wei-Han,Chen, Xin-Zhi

, p. 1208 - 1212 (2011/05/30)

cis-(3R,4R)-N-(tert-Butoxycarbonyl)-4-methyl-3-(methylamino)piperidine, a key intermediate for the synthesis of CP-690550 (a potent protein kinase inhibitor), is prepared via an asymmetric approach starting from ethyl 1-benzyl-3-oxopiperidine-4-carboxylat

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