41980-31-8

Usage

Uses

Used in Pharmaceutical Industry:
PIPERIDINE-2,6-DICARBONITRILE is used as a key building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure and reactivity allow for the creation of diverse medicinal compounds with potential applications in treating various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, PIPERIDINE-2,6-DICARBONITRILE serves as an essential intermediate in the production of agrochemicals. Its incorporation into these compounds aids in the development of effective pesticides, herbicides, and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used in Fine Chemicals Industry:
PIPERIDINE-2,6-DICARBONITRILE is utilized as a versatile intermediate in the synthesis of fine chemicals. Its presence in these compounds enables the production of high-quality specialty chemicals used in various applications, such as fragrances, dyes, and other industrial processes.
Used in Heterocyclic and Aliphatic Derivatives Production:
PIPERIDINE-2,6-DICARBONITRILE is employed as a crucial intermediate in the synthesis of heterocyclic and aliphatic derivatives. Its involvement in the production of these compounds expands the range of chemical structures available for use in various industries, including pharmaceuticals, agrochemicals, and materials science.

InChI:InChI=1/C7H9N3/c8-4-6-2-1-3-7(5-9)10-6/h6-7,10H,1-3H2

Upstream product

• 143-33-9 sodium cyanide 
• 111-30-8 Glutaraldehyde 
• 22905-25-5 N-nitroso-2,6-dicyanopiperidine 
• 74-90-8 hydrogen cyanide 

Downstream Products

• 22905-25-5 N-nitroso-2,6-dicyanopiperidine 
• 99669-83-7 piperidine-2,6-dicarboxamide 
• 98493-09-5 6-carbamoyl-piperidine-2-carboxylic acid methyl ester 
• 41980-32-9 5,5'-trimethylenedihydantoin 
• 14289-34-0 (S,S)-2,6-diaminopimelic acid 
• 922-54-3 2,6-diaminopimelic acid 
• 42920-79-6 meso-2,6-dibenzyloxycarbonylaminopimelic acid 
• 20714-84-5 L-2,6-dibenzyloxycarbonylaminopimelic acid 
• 20714-74-3 rac-2,6-dibenzyloxycarbonylaminopimelic acid 
• 78082-26-5 N⁶-benzyloxycarbonyl-L-2,6-diaminopimelamic acid 
• 78057-66-6 L-2,6-diaminopimelamic acid dichlorhydrate 
• 78088-48-9 L-2,6-dibenzyloxycarbonylaminopimelamic acid 
• 121190-51-0 O¹-p-nitrobenzyl-N²-benzyloxycarbonyl-L-2,6-diaminopimelic acid 
• 78057-77-9 RP 56142 

Relevant academic research and scientific papers

2,6-BIS-(AMINOMETHYL)PIPERIDINE DERIVATIVES

The present invention relates to 2,6-bis(aminomethyl)piperidine derivatives as such (in the following text abbreviated to “2,6-BAMP derivatives”) which are defined by the general formula (I) shown in the following text. In addition, the present invention relates to a process for preparing such 2,6-BAMP derivatives by hydrogenation of the corresponding 2,6-dicyanopiperidine derivatives (hereinafter abbreviated to “2,6-DCP derivatives”) in the presence of a catalyst. The present invention further provides for the use of the 2,6-BAMP derivatives of the invention as hardeners for epoxy resins, as intermediate in the preparation of diisocyanates, which play an important role in the production of polyurethanes, as starters in the preparation of polyetherols and/or as monomers for polyamide production. The present invention further relates to the diisocyanates as such prepared from the 2,6-BAMP derivatives and also the corresponding preparative process.

Processes for preparing intermediates of inhibitors of enkephalinase and angiotensin converting enzyme and intermediates thereof

The present invention relates to novel processes for preparing intermediates of the formula I STR1 and to novel intermediates thereof which are useful in the preparation of inhibitors of enkephalinase and angiotensin converting enzyme.

Alicyclic Nitrosamines and Nitrosamino Acids as Transnitrosating Agents

Many alicyclic nitrosamines act as nitrosating agents under mild conditions (pH 1-3, in the presence of nucleophilic catalysts such as thiocyanate).All nitrosopiperazines, nitrosomorpholines, and nitrosamino acids tested were found to act as nitrosating agents, and certain nitrosopiperidines also showed this capability.Acyclic nitrosamines are far less reactive than functionally similar cyclic compounds.