Home Other Building Blocks 2-Methyl-1H-pyrrole

2-Methyl-1H-pyrrole

CAS No.:
636-41-9
Catalog Number:
AG0035W2
Molecular Formula:
C5H7N
Molecular Weight:
81.1158
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
96%
In Stock USA
United States
$18
- +
5g
96%
In Stock USA
United States
$69
- +
25g
96%
In Stock USA
United States
$310
- +
100g
96%
In Stock USA
United States
$1050
- +
Product Description
Catalog Number:
AG0035W2
Chemical Name:
2-Methyl-1H-pyrrole
CAS Number:
636-41-9
Molecular Formula:
C5H7N
Molecular Weight:
81.1158
MDL Number:
MFCD02822910
IUPAC Name:
2-methyl-1H-pyrrole
InChI:
InChI=1S/C5H7N/c1-5-3-2-4-6-5/h2-4,6H,1H3
InChI Key:
TVCXVUHHCUYLGX-UHFFFAOYSA-N
SMILES:
Cc1ccc[nH]1
EC Number:
211-255-4
UNII:
486RY4814O
NSC Number:
81346
Properties
Complexity:
43.2  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
81.058g/mol
Formal Charge:
0
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
81.118g/mol
Monoisotopic Mass:
81.058g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  
Literature
Title Journal
Precursors and nitrogen origins of trichloronitromethane and dichloroacetonitrile during chlorination/chloramination. Chemosphere 20120601
(1H-Pyrrol-2-ylmethylidene)(3-{[(1H-pyrrol-2-ylmethylidene)amino]methyl}benzyl)amine. Acta crystallographica. Section E, Structure reports online 20101201
Regioselective formation of alpha-vinylpyrroles from the ruthenium-catalyzed coupling reaction of pyrroles and terminal alkynes involving C-H bond activation. The Journal of organic chemistry 20100507
Two new tropane alkaloids from the bark of Erythroxylum vacciniifolium Mart. (Erythroxylaceae). Natural product communications 20091001
Metabolism of 5-isopropyl-6-(5-methyl-1,3,4-oxadiazol-2-yl)-N-(2-methyl-1H-pyrrolo[2,3-b]pyridin-5-yl)pyrrolo[2,1-f][1,2,4]triazin-4-amine (BMS-645737): identification of an unusual N-acetylglucosamine conjugate in the cynomolgus monkey. Drug metabolism and disposition: the biological fate of chemicals 20081201
Alkyl peroxides reveal the ring opening mechanism of verdoheme catalyzed by heme oxygenase. Journal of the American Chemical Society 20080402
Methylpyrrole tropane alkaloids from the bark of Erythroxylum vacciniifolium. Journal of natural products 20050801
Electronic structures of five-coordinate iron(III) porphyrin complexes with highly ruffled porphyrin ring. Inorganic chemistry 20040809
Importance of the C-H...N weak hydrogen bonding on the coordination structures of manganese(III) porphyrin complexes. Inorganic chemistry 20030407
Retinoic acid metabolism inhibition by 3-azolylmethyl-1H-indoles and 2, 3 or 5-(alpha-azolylbenzyl)-1H-indoles. Journal of enzyme inhibition and medicinal chemistry 20030401
Minor groove DNA binders as antimicrobial agents. 1. Pyrrole tetraamides are potent antibacterials against vancomycin resistant Enterococci [corrected] and methicillin resistant Staphylococcus aureus. Journal of medicinal chemistry 20020214
Properties