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72864-28-9

72864-28-9 | 2-Oxo-2,3-dihydro-1H-imidazole-4-carbaldehyde

CAS No: 72864-28-9 Catalog No: AG005E7U MDL No:MFCD01314543

Product Description

Catalog Number:
AG005E7U
Chemical Name:
2-Oxo-2,3-dihydro-1H-imidazole-4-carbaldehyde
CAS Number:
72864-28-9
Molecular Formula:
C4H4N2O2
Molecular Weight:
112.0868
MDL Number:
MFCD01314543
IUPAC Name:
2-oxo-1,3-dihydroimidazole-4-carbaldehyde
InChI:
InChI=1S/C4H4N2O2/c7-2-3-1-5-4(8)6-3/h1-2H,(H2,5,6,8)
InChI Key:
XYBQLONABMMZQU-UHFFFAOYSA-N
SMILES:
O=Cc1c[nH]c(=O)[nH]1

Properties

Complexity:
161  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
112.027g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
112.088g/mol
Monoisotopic Mass:
112.027g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
58.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.2  

Literature

Title Journal
Cloning, reassembling and integration of the entire nikkomycin biosynthetic gene cluster into Streptomyces ansochromogenes lead to an improved nikkomycin production. Microbial cell factories 20100101
Selectively improving nikkomycin Z production by blocking the imidazolone biosynthetic pathway of nikkomycin X and uracil feeding in Streptomyces ansochromogenes. Microbial cell factories 20090101
Identification and characterization of sanH and sanI involved in the hydroxylation of pyridyl residue during nikkomycin biosynthesis in Streptomyces ansochromogenes. Current microbiology 20071201
Synthesis of 4-formyl-4-imidazolin-2-one nucleosides, isomers of uridine and 2'-deoxyuridine. Nucleosides, nucleotides & nucleic acids 20040101

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