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
One-step synthesis of triethynylvinylmethanes and tetraethynylmethanes by GaCl(3)-promoted diethynylation of 1,4-enynes and 1,4-diynes.	2005 Jun 15	15941236
Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives.	2006 Nov 9	17078715
PIKfyve regulation of endosome-linked pathways.	2009 Jul	19582903

Patents

Substance Class	Chemical Created by `admin` on `Sat Dec 16 03:04:23 GMT 2023` Edited by `admin` on `Sat Dec 16 03:04:23 GMT 2023`
Record UNII	83004E89V5
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

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

NSC-175792

Code

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