Home Aldehydes 3-Furaldehyde

3-Furaldehyde

CAS No.:
498-60-2
Catalog Number:
AG003JI7
Molecular Formula:
C5H4O2
Molecular Weight:
96.0841
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$32
- +
5g
97%
In Stock USA
United States
$119
- +
25g
97%
In Stock USA
United States
$475
- +
Product Description
Catalog Number:
AG003JI7
Chemical Name:
3-Furaldehyde
CAS Number:
498-60-2
Molecular Formula:
C5H4O2
Molecular Weight:
96.0841
MDL Number:
MFCD00010424
IUPAC Name:
furan-3-carbaldehyde
InChI:
InChI=1S/C5H4O2/c6-3-5-1-2-7-4-5/h1-4H
InChI Key:
AZVSIHIBYRHSLB-UHFFFAOYSA-N
SMILES:
O=Cc1cocc1
UNII:
POB632X444
Properties
Complexity:
70.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
96.021g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
96.085g/mol
Monoisotopic Mass:
96.021g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
30.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
Tetrabutylammonium fluoride (TBAF)-catalyzed addition of substituted trialkylsilylalkynes to aldehydes, ketones, and trifluoromethyl ketones. The Journal of organic chemistry 20110603
Neonicotinoid insecticides: oxidative stress in planta and metallo-oxidase inhibition. Journal of agricultural and food chemistry 20110511
Photoisomerization and photochemistry of matrix-isolated 3-furaldehyde. The journal of physical chemistry. A 20101202
Adsorption and separation of reactive aromatic isomers and generation and stabilization of their radicals within cadmium(II)-triazole metal-organic confined space in a single-crystal-to-single-crystal fashion. Journal of the American Chemical Society 20100526
A direct RP-HPLC method for the determination of furanic aldehydes and acids in honey. Talanta 20090415
Total synthesis of 20-norsalvinorin A. 1. Preparation of a key intermediate. The Journal of organic chemistry 20090320
Synthesis of heteroaryl imines: theoretical and experimental approach to the determination of the configuration of C=N double bond. The Journal of organic chemistry 20060915
Synthesis of new lipophilic ipomeanol analogues and their cytotoxic activities. Archiv der Pharmazie 20050101
[Studies on the chemical constituents of the volatiles of Clerodendron bungei]. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20040201
Synthesis of (+)-manoalide via a copper(I)-mediated 1,2-metalate rearrangement. The Journal of organic chemistry 20030516
Properties