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64951-36-6

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64951-36-6 Usage

Description

4-Aminocarbethoxypiperidine, with the molecular formula C9H16N2O2, is a chemical compound that features a piperidine ring and an amino group. It is a small molecule known for its role as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique properties and reactivity make it a valuable component in medicinal chemistry, particularly for the preparation of bioactive molecules.

Uses

Used in Pharmaceutical Synthesis:
4-Aminocarbethoxypiperidine is used as a building block for the preparation of bioactive molecules, contributing to the development of new pharmaceuticals. Its presence in the molecular structure of various compounds allows for the exploration of its potential therapeutic effects and applications in medicine.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 4-aminocarbethoxypiperidine is utilized as an intermediate for the synthesis of a wide range of organic compounds. Its reactivity and structural features make it a versatile component in the creation of diverse chemical entities.
Used in Medicinal Chemistry Research and Development:
4-Aminocarbethoxypiperidine is a significant focus of research and development within the realm of medicinal chemistry. Its potential applications in the production of drugs and other organic compounds drive ongoing studies to uncover its full capabilities and optimize its use in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 64951-36-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,5 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 64951-36:
(7*6)+(6*4)+(5*9)+(4*5)+(3*1)+(2*3)+(1*6)=146
146 % 10 = 6
So 64951-36-6 is a valid CAS Registry Number.

64951-36-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H63095)  4-(Ethoxycarbonylamino)piperidine, 97%   

  • 64951-36-6

  • 250mg

  • 221.0CNY

  • Detail
  • Alfa Aesar

  • (H63095)  4-(Ethoxycarbonylamino)piperidine, 97%   

  • 64951-36-6

  • 1g

  • 706.0CNY

  • Detail
  • Alfa Aesar

  • (H63095)  4-(Ethoxycarbonylamino)piperidine, 97%   

  • 64951-36-6

  • 5g

  • 2940.0CNY

  • Detail

64951-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-aminoethyl piperidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names Carbamic acid,N-4-piperidinyl-,ethyl ester

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:64951-36-6 SDS

64951-36-6Downstream Products

64951-36-6Relevant articles and documents

Carbostyril compounds connected via an oxyalkyl group with a piperidine ring and having pharmaceutical utility

-

, (2008/06/13)

Carbostyril derivatives of Formula I: STR1 wherein: m is 0, 1, or 2; n is 0, 1, or 2; R1 is hydrogen or lower alkyl; R2 is hydrogen, halogen, hydroxy, lower alkyl, lower alkoxy, aralkoxy, or acyloxy; R3 is hydrogen, halogen, lower alkyl, or lower alkoxy; R4 is hydrogen, hydroxy, lower alkyl, acyloxy, provided that when R4 is hydroxy or acyloxy, m and n are both 1; R5 is hydrogen or lower alkyl; and R6 is alkyl, hydroxyalkyl, alkoxyalkyl, or (dialkylamino)alkyl; and the pharmaceutically acceptable acid addition salts and N-oxides (at the carbostyril nitrogen) thereof, and compositions containing them, are useful in treating cardiovascular diseases, particularly arrhythmias. Methods of preparing intermediates, the compounds, their formulations and methods of treatment therewith are also disclosed.

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