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Cycloheptanol

CAS No.:
502-41-0
Catalog Number:
AG0034NE
Molecular Formula:
C7H14O
Molecular Weight:
114.1855
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$111
- +
5g
98%
In Stock USA
United States
$126
- +
25g
98%
In Stock USA
United States
$179
- +
Product Description
Catalog Number:
AG0034NE
Chemical Name:
Cycloheptanol
CAS Number:
502-41-0
Molecular Formula:
C7H14O
Molecular Weight:
114.1855
MDL Number:
MFCD00004150
IUPAC Name:
cycloheptanol
InChI:
InChI=1S/C7H14O/c8-7-5-3-1-2-4-6-7/h7-8H,1-6H2
InChI Key:
QCRFMSUKWRQZEM-UHFFFAOYSA-N
SMILES:
OC1CCCCCC1
EC Number:
207-936-0
NSC Number:
52221
Properties
Complexity:
53.4  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
114.104g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
114.188g/mol
Monoisotopic Mass:
114.104g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1  
Literature
Title Journal
Disentangling the secondary relaxations in the orientationally disordered mixed crystals: cycloheptanol + cyclooctanol two-component system. The journal of physical chemistry. B 20100513
Highly substituted benzannulated cyclooctanol derivatives by samarium diiodide-induced cyclizations. Beilstein journal of organic chemistry 20100101
Study of supercooled orientationally disordered binary solid solutions II: cyclohexyl derivatives, neopentanol and neopentylglycol. Physical chemistry chemical physics : PCCP 20091028
Dielectric and calorimetric study of orientationally disordered phases in two unusual two-component systems. The journal of physical chemistry. B 20080306
Fluorescent detection for cyclic and acyclic alcohol guests by naphthalene-appended amino-beta-cyclodextrins. Organic letters 20061026
Thermodynamics of the molecular and chiral recognition of cycloalkanols and camphor by modified beta-cyclodextrins possessing simple aromatic tethers. The Journal of organic chemistry 20040109
[Lipase-catalyzed kinetic resolution of 2-substituted cycloalkanols]. Acta pharmaceutica Hungarica 20010101
Properties