Home Other Building Blocks 2,5-Dimethylpyrrole

2,5-Dimethylpyrrole

CAS No.:
625-84-3
Catalog Number:
AG00330L
Molecular Formula:
C6H9N
Molecular Weight:
95.1424
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$25
- +
25g
98%
In Stock USA
United States
$82
- +
100g
98%
In Stock USA
United States
$263
- +
Product Description
Catalog Number:
AG00330L
Chemical Name:
2,5-Dimethylpyrrole
CAS Number:
625-84-3
Molecular Formula:
C6H9N
Molecular Weight:
95.1424
MDL Number:
MFCD00005223
IUPAC Name:
2,5-dimethyl-1H-pyrrole
InChI:
InChI=1S/C6H9N/c1-5-3-4-6(2)7-5/h3-4,7H,1-2H3
InChI Key:
PAPNRQCYSFBWDI-UHFFFAOYSA-N
SMILES:
Cc1ccc([nH]1)C
EC Number:
210-913-8
UNII:
MZ3OYF5521
NSC Number:
4507
Properties
Complexity:
53.2  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
95.073g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
95.145g/mol
Monoisotopic Mass:
95.073g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
Title Journal
Direct functionalization of (un)protected tetrahydroisoquinoline and isochroman under iron and copper catalysis: two metals, two mechanisms. The Journal of organic chemistry 20111104
Hydrogen-bonded structures for self-aggregates of 2,5-dimethylpyrrole and its binary clusters with pyrrole studied by IR cavity ringdown spectroscopy. Physical chemistry chemical physics : PCCP 20110821
Ligand substitution from the (eta5-DMP)Mn(CO)2(Solv) [DMP = 2,5-dimethylpyrrole, Solv = solvent] complexes: to ring slip or not to ring slip? Inorganic chemistry 20100816
Comparison of the resonance-enhanced multiphoton ionization spectra of pyrrole and 2,5-dimethylpyrrole: Building toward an understanding of the electronic structure and photochemistry of porphyrins. The Journal of chemical physics 20091107
2,2',5,5'-Tetra-methyl-1,1'-(hexane-1,6-di-yl)di-1H-pyrrole. Acta crystallographica. Section E, Structure reports online 20090701
Fundamental studies of tungsten alkylidene imido monoalkoxidepyrrolide complexes. Journal of the American Chemical Society 20090610
Comparative covalent protein binding of 2,5-hexanedione and 3-acetyl-2,5-hexanedione in the rat. Journal of toxicology and environmental health. Part A 20090101
Conversion of methane to liquid products, hydrogen, and ammonia with environmentally friendly condition-based microgap discharge. Journal of the Air & Waste Management Association (1995) 20081201
Molybdenum tris(2,5-dimethylpyrrolide), a rare homoleptic molybdenum(III) monomer. Inorganic chemistry 20081117
Synthesis of bifunctional imido alkylidene bispyrrolide complexes of molybdenum and their conversion into bifunctional imido alkylidene diolate complexes that can be employed as ROMP initiators. Chemistry, an Asian journal 20080901
Synthesis, cannabinoid receptor affinity, and molecular modeling studies of substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides. Journal of medicinal chemistry 20080327
High resolution photofragment translational spectroscopy studies of the near ultraviolet photolysis of 2,5-dimethylpyrrole. Physical chemistry chemical physics : PCCP 20060207
A new class of potent non-imidazole H(3) antagonists: 2-aminoethylbenzofurans. Bioorganic & medicinal chemistry letters 20040209
Effect of the pyrrole polymerization mechanism on the antioxidative activity of nonenzymatic browning reactions. Journal of agricultural and food chemistry 20030910
Protection of the amino group of adenosine and guanosine derivatives by elaboration into a 2,5-dimethylpyrrole moiety. Organic letters 20030904
Poor metabolization of n-hexane in Parkinson's disease. Journal of neurology 20030501
Evidence of zinc protection against 2,5-hexanedione neurotoxicity: correlation of neurobehavioral testing with biomarkers of excretion. Neurotoxicology 20021201
Properties