Home Aldehydes Pyrimidine-5-carboxaldehyde

Pyrimidine-5-carboxaldehyde

CAS No.:
10070-92-5
Catalog Number:
AG0002O7
Molecular Formula:
C5H4N2O
Molecular Weight:
108.0981
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$25
- +
5g
97%
In Stock USA
United States
$88
- +
10g
97%
In Stock USA
United States
$169
- +
25g
97%
In Stock USA
United States
$357
- +
100g
97%
In Stock USA
United States
$1082
- +
Product Description
Catalog Number:
AG0002O7
Chemical Name:
Pyrimidine-5-carboxaldehyde
CAS Number:
10070-92-5
Molecular Formula:
C5H4N2O
Molecular Weight:
108.0981
MDL Number:
MFCD03426065
IUPAC Name:
pyrimidine-5-carbaldehyde
InChI:
InChI=1S/C5H4N2O/c8-3-5-1-6-4-7-2-5/h1-4H
InChI Key:
FREJAOSUHFGDBW-UHFFFAOYSA-N
SMILES:
O=Cc1cncnc1
Properties
Complexity:
78.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
108.032g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
108.1g/mol
Monoisotopic Mass:
108.032g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
42.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.3  
Literature
Title Journal
Asymmetric autocatalysis: triggered by chiral isotopomer arising from oxygen isotope substitution. Angewandte Chemie (International ed. in English) 20110822
Enantioselective C-C bond formation as a result of the oriented prochirality of an achiral aldehyde at the single-crystal face upon treatment with a dialkyl zinc vapor. Angewandte Chemie (International ed. in English) 20110718
Asymmetric autocatalysis induced by chiral crystals of achiral tetraphenylethylenes. Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life 20100201
Discrimination of cryptochirality in chiral isotactic polystyrene by asymmetric autocatalysis. Chemical communications (Cambridge, England) 20091007
Asymmetric autocatalysis induced by meteoritic amino acids with hydrogen isotope chirality. Chemical communications (Cambridge, England) 20090807
Abstracts of the 2008 ISSOL Meeting. August 24-29, 2008. Florence, Italy. Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life 20090801
Asymmetric autocatalysis triggered by carbon isotope (13C/12C) chirality. Science (New York, N.Y.) 20090424
Highly enantioselective asymmetric autocatalysis using chiral ruthenium complex-ion-exchanged synthetic hectorite as a chiral initiator. Organic & biomolecular chemistry 20090321
Spontaneous absolute asymmetric synthesis in the presence of achiral silica gel in conjunction with asymmetric autocatalysis. Chirality 20060801
Chiral discrimination of cryptochiral saturated quaternary and tertiary hydrocarbons by asymmetric autocatalysis. Journal of the American Chemical Society 20060510
Asymmetric autocatalysis induced by chiral hydrocarbon [2.2]paracyclophanes. Organic & biomolecular chemistry 20030121
Asymmetric autocatalysis and its application to chiral discrimination. Chirality 20020701
Synthesis and muscarinic activity of 1,2,3,4-tetrahydropyrimidine derivatives. Archiv der Pharmazie 20010301
Asymmetric autocatalysis and the origin of chiral homogeneity in organic compounds. Chemical record (New York, N.Y.) 20010101
Properties