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4501-58-0 | 3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-, (1R)-
CAS No: 4501-58-0 Catalog No: AG01DNTM MDL No:MFCD00274368
Product Description
Catalog Number:
AG01DNTM
Chemical Name:
3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-, (1R)-
CAS Number:
4501-58-0
MDL Number:
MFCD00274368
IUPAC Name:
2-(2,2,3-trimethylcyclopent-3-en-1-yl)acetaldehyde
InChI:
InChI=1S/C10H16O/c1-8-4-5-9(6-7-11)10(8,2)3/h4,7,9H,5-6H2,1-3H3
InChI Key:
OGCGGWYLHSJRFY-UHFFFAOYSA-N
EC Number:
224-815-8
FEMA Number:
3592
Properties
Complexity:
189
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
152.12g/mol
Formal Charge:
0
Heavy Atom Count:
11
Hydrogen Bond Acceptor Count:
1
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
152.237g/mol
Monoisotopic Mass:
152.12g/mol
Rotatable Bond Count:
2
Topological Polar Surface Area:
17.1A^2
Undefined Atom Stereocenter Count:
1
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9
Literature
| Title | Journal |
|---|---|
| Denuder sampling techniques for the determination of gas-phase carbonyl compounds: a comparison and characterisation of in situ and ex situ derivatisation methods. | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110515 |
| Laboratory chamber studies on the formation of organosulfates from reactive uptake of monoterpene oxides. | Physical chemistry chemical physics : PCCP 20090928 |
| Phosphotungstic acid as a versatile catalyst for the synthesis of fragrance compounds by alpha-pinene oxide isomerization: solvent-induced chemoselectivity. | Chemistry (Weinheim an der Bergstrasse, Germany) 20080101 |
| Probing the Lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). | Chemistry (Weinheim an der Bergstrasse, Germany) 20060925 |
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