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254905-64-1

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254905-64-1 Usage

Description

(S)-3-(Dimethylaminomethyl)-N-boc-piperidine is a chemical compound consisting of a piperidine ring with a dimethylaminomethyl group and a Boc (tert-butoxycarbonyl) protecting group. (S)-3-(Dimethylaminomethyl)-N-boc-piperidine is characterized by its unique molecular structure and properties, which make it a promising candidate for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.

Uses

Used in Pharmaceutical Industry:
(S)-3-(Dimethylaminomethyl)-N-boc-piperidine is used as a building block in organic synthesis for the preparation of various pharmaceuticals. Its unique molecular structure, including the dimethylaminomethyl group and the Boc protecting group, allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (S)-3-(Dimethylaminomethyl)-N-boc-piperidine is used as a key component in the synthesis of various agrochemicals. Its basic properties, conferred by the dimethylaminomethyl group, can be exploited in the development of new compounds with pesticidal, herbicidal, or other agricultural applications.
Used in Materials Science:
(S)-3-(Dimethylaminomethyl)-N-boc-piperidine also has potential applications in materials science. Its unique molecular structure and properties can be utilized in the development of new materials with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance.
Overall, (S)-3-(Dimethylaminomethyl)-N-boc-piperidine is a versatile compound with a wide range of potential applications across different industries, thanks to its unique molecular structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 254905-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,9,0 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 254905-64:
(8*2)+(7*5)+(6*4)+(5*9)+(4*0)+(3*5)+(2*6)+(1*4)=151
151 % 10 = 1
So 254905-64-1 is a valid CAS Registry Number.

254905-64-1SDS

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 3-[(dimethylamino)methyl]piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names (S)-TERT-BUTYL 3-((DIMETHYLAMINO)METHYL)PIPERIDINE-1-CARBOXYLATE

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:254905-64-1 SDS

254905-64-1Relevant articles and documents

THERAPEUTIC ISOXAZOLE COMPOUNDS

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Page/Page column 42, (2009/04/24)

The invention provides a compound of formula I: wherein A1, A2, A3, R1, X, Y, and B have any of the values described herein, as well as salts of such compounds, compositions comprising such compounds, and therapeutic methods that comprise the administration of such compounds. The compounds are inhibitors of monoamine oxidase B (MAO-B) enzyme function and are useful for improving cognitive function and for treating psychiatric disorders in animals.

The influence of conformational restriction in the C-terminus of growth hormone secretagogues on their potency

Peschke, Bernd,Ankersen, Michael,Bauer, Michael,Hansen, Thomas Kruse,Hansen, Birgit Sehested,Nielsen, Karin Kramer,Raun, Kirsten,Richter, Lutz,Westergaard, Lisbet

, p. 487 - 501 (2007/10/03)

In order to obtain more potent growth hormone secretagogues, a comparison of ipamorelin and NN703 suggested the addition of a polar group at the C-terminus of NN703. A study was conducted using constrained amines for this purpose. Here, substituted 4-piperidinylamino- and 4-dimethylaminopiperidino-substitutents were found to give the most active compounds. A replacement of the 4-dimethylaminopiperidino-substituent with 4-hydroxypiperidino resulted in a series of compounds, which showed in vitro activity with EC50 values in the low nanomolar range, and favourable kinetic properties, such as 40% oral bioavailability. The most promising compound was also tested in a swine in vivo model, resulting in a growth hormone level with a Cmax of over 40 ng mL-1.

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