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(2R,6R)-2,6-DIALLYL-1,2,3,6-TETRAHYDROPYRIDINE is a tetrahydropyridine derivative with the molecular formula C12H17N. It features two allyl groups attached to the nitrogen atom, giving it a unique structure that holds potential for applications in organic synthesis and pharmaceuticals. This chemical compound may also possess biological activities, making it a subject of interest for researchers in medicine and pharmacology.

138617-50-2

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138617-50-2 Usage

Uses

Used in Organic Synthesis:
(2R,6R)-2,6-DIALLYL-1,2,3,6-TETRAHYDROPYRIDINE is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for the development of new compounds with potential applications in different fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2R,6R)-2,6-DIALLYL-1,2,3,6-TETRAHYDROPYRIDINE is used as a precursor in the synthesis of drugs. Its specific structure can be leveraged to design and develop new pharmaceuticals with targeted therapeutic effects.
Used in Medicinal Research:
(2R,6R)-2,6-DIALLYL-1,2,3,6-TETRAHYDROPYRIDINE is utilized in medicinal research as a compound of interest for its potential biological activities. Researchers explore its interactions with biological systems to understand its effects and possible uses in treating diseases or conditions.
Used in Drug Development:
As a component in drug development, (2R,6R)-2,6-DIALLYL-1,2,3,6-TETRAHYDROPYRIDINE is used to create new pharmaceutical agents. Its unique properties may contribute to the discovery of novel drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 138617-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,1 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138617-50:
(8*1)+(7*3)+(6*8)+(5*6)+(4*1)+(3*7)+(2*5)+(1*0)=142
142 % 10 = 2
So 138617-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H17N/c1-3-6-10-8-5-9-11(12-10)7-4-2/h3-5,8,10-12H,1-2,6-7,9H2/t10-,11-/m1/s1

138617-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,6R)-2,6-bis(prop-2-enyl)-1,2,3,6-tetrahydropyridine

1.2 Other means of identification

Product number -
Other names trans-2,6-diallyl-1,2,5,6-tetrahydropyridine

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:138617-50-2 SDS

138617-50-2Relevant academic research and scientific papers

Reductive trans-2,6-diallylation of pyridines with allylboranes. Synthesis of trans- and cis-2,6-diallyl-1,2,5,6-tetrahydropyridines and their deuterated derivatives

Bubnov, Yu. N.,Shagova, E. A.,Evchenko, S. V.,Ignatenko, A. V.

, p. 645 - 656 (1994)

The reductive trans-2,6-diallylation of pyridines with trialllyl and allyl(dialkyl)boranes has been discovered.Heating (40-100 deg C) of pyridine, deuteropyridine, or 3-bromopyridine complexes with triallylborane in the presence of alcohols (ROH or CH3OD)

New growth regulators of corn based on N-mono- and N,N-bis-3-butenyldichloroacetamides

Bubnov, Yu. N.,Spiridonov, Yu. Ya.,Kuznetsov, N. Yu.

, p. 345 - 358 (2018/05/22)

Allylboration of imines, nitriles (including hydrocyanic acid), amides, lactams, aromatic azaheterocycles (pyridines, isoquinoline, and pyrrole) was used to synthesize a series of mono- and bis-3-butenylamines with different structures, which were converted to dichloroacetamides, new analogs of a known safener (herbicide antidote) Dichlormid successfully used in the cultivation of corn throughout the world. Biological tests for the germination of corn seeds showed that most of the dichloroacetamides obtained have growth-stimulating activity, which is mainly directed on the development of the root system. Compounds 2f, trans- and cis-2n, cis-2s, and 2t demonstrated outstanding activity, exceeding from two to three times the stimulating effect of Dichlormid on the developing root system of maize seedlings.

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