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Home Other Building Blocks 1H-Pyrrole, 2-undecyl-

1H-Pyrrole, 2-undecyl-

CAS No.:
61930-40-3
Catalog Number:
AG0038LF
Molecular Formula:
C15H27N
Molecular Weight:
221.3816
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Product Description
Catalog Number:
AG0038LF
Chemical Name:
1H-Pyrrole, 2-undecyl-
CAS Number:
61930-40-3
Molecular Formula:
C15H27N
Molecular Weight:
221.3816
IUPAC Name:
2-undecyl-1H-pyrrole
InChI:
InChI=1S/C15H27N/c1-2-3-4-5-6-7-8-9-10-12-15-13-11-14-16-15/h11,13-14,16H,2-10,12H2,1H3
InChI Key:
LIZHBNXWXKXCEF-UHFFFAOYSA-N
SMILES:
CCCCCCCCCCCc1[nH]ccc1
Properties
Complexity:
144  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
221.214g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
221.388g/mol
Monoisotopic Mass:
221.214g/mol
Rotatable Bond Count:
10  
Topological Polar Surface Area:
15.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
7.6  
Literature
Title Journal
Stereochemical elucidation of streptorubin B. Journal of the American Chemical Society 20110216
Role and substrate specificity of the Streptomyces coelicolor RedH enzyme in undecylprodiginine biosynthesis. Chemical communications (Cambridge, England) 20080428
Elucidation of the Streptomyces coelicolor pathway to 2-undecylpyrrole, a key intermediate in undecylprodiginine and streptorubin B biosynthesis. Chemistry & biology 20080201
Biosynthesis of the red antibiotic, prodigiosin, in Serratia: identification of a novel 2-methyl-3-n-amyl-pyrrole (MAP) assembly pathway, definition of the terminal condensing enzyme, and implications for undecylprodigiosin biosynthesis in Streptomyces. Molecular microbiology 20050501
Properties