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38222-83-2

38222-83-2 | 2,6-Di-Tert-Butyl-4-Methylpyridine

CAS No: 38222-83-2 Catalog No: AG003322 MDL No:MFCD00006305

Product Description

Catalog Number:
AG003322
Chemical Name:
2,6-Di-Tert-Butyl-4-Methylpyridine
CAS Number:
38222-83-2
Molecular Formula:
C14H23N
Molecular Weight:
205.3391
MDL Number:
MFCD00006305
IUPAC Name:
2,6-ditert-butyl-4-methylpyridine
InChI:
InChI=1S/C14H23N/c1-10-8-11(13(2,3)4)15-12(9-10)14(5,6)7/h8-9H,1-7H3
InChI Key:
HVHZEKKZMFRULH-UHFFFAOYSA-N
SMILES:
Cc1cc(nc(c1)C(C)(C)C)C(C)(C)C
EC Number:
253-834-4
UNII:
83004E89V5
NSC Number:
175792

Properties

Complexity:
184  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
205.183g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
205.345g/mol
Monoisotopic Mass:
205.183g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
12.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.6  

Literature

Title Journal
PIKfyve regulation of endosome-linked pathways. Traffic (Copenhagen, Denmark) 20090701
Cyclization reactions of homopropargyl azide derivatives catalyzed by PtCl4 in ethanol solution: synthesis of functionalized pyrrole derivatives. Organic letters 20061109
One-step synthesis of triethynylvinylmethanes and tetraethynylmethanes by GaCl(3)-promoted diethynylation of 1,4-enynes and 1,4-diynes. Journal of the American Chemical Society 20050615
Adduct formation of methyltrioxorhenium with mono- and bidentate nitrogen donors: formation constants. Inorganic chemistry 20030630
New cationic olefin cyclization-pinacol reactions. Ring-expanding cyclopentane annulations that directly install useful functionality in the cyclopentane ring. The Journal of organic chemistry 20020906
GaCl(3)-catalyzed ortho-ethynylation of phenols. Journal of the American Chemical Society 20020724

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