2,6-DI-TERT-BUTYL-4-METHYLPYRIDINE

CC1=CC(=NC(=C1)C(C)(C)C)C(C)(C)C

InChIKey=HVHZEKKZMFRULH-UHFFFAOYSA-N

InChI=1S/C14H23N/c1-10-8-11(13(2,3)4)15-12(9-10)14(5,6)7/h8-9H,1-7H3

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

PubMed

Title	Date	PubMed
PIKfyve regulation of endosome-linked pathways.	2009-07	19582903
Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives.	2006-11-09	17078715
One-step synthesis of triethynylvinylmethanes and tetraethynylmethanes by GaCl(3)-promoted diethynylation of 1,4-enynes and 1,4-diynes.	2005-06-15	15941236
Adduct formation of methyltrioxorhenium with mono- and bidentate nitrogen donors: formation constants.	2003-06-30	12817981
New cationic olefin cyclization-pinacol reactions. Ring-expanding cyclopentane annulations that directly install useful functionality in the cyclopentane ring.	2002-09-06	12201763
GaCl(3)-catalyzed ortho-ethynylation of phenols.	2002-07-24	12121084

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:16:26 GMT 2025` Edited by `admin` on `Mon Mar 31 21:16:26 GMT 2025`
Record UNII	83004E89V5
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

NSC-175792

Preferred Name

English

2,6-DI-TERT-BUTYL-4-METHYLPYRIDINE

Systematic Name

English

2,6-DI-TERT-BUTYL-4-METHYLPYRIDINE [MI]

Common Name

English

IDINE, 2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-

Common Name

English

DTBMP

Common Name

English

4-METHYL-2,6-DI-TERT-BUTYLPYRIDINE

Systematic Name

English

2,6-DI-TERT-BUTYL-4-PICOLINE

Common Name

English

2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYLPYRIDINE

Systematic Name

English

Code System Code Type Description

PUBCHEM

98898