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100-49-2,MFCD00001510
Catalog No.:AA00003E
Cyclohexanemethanol | 100-49-2
Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$10.00
- +
25g
97%
in stock  
$15.00
- +
100g
97%
in stock  
$50.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00003E
Chemical Name:
Cyclohexanemethanol
CAS Number:
100-49-2
Molecular Formula:
C7H14O
Molecular Weight:
114.1855
MDL Number:
MFCD00001510
IUPAC Name:
cyclohexylmethanol
InChI:
InChI=1S/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2
InChI Key:
VSSAZBXXNIABDN-UHFFFAOYSA-N
SMILES:
OCC1CCCCC1
EC Number:
202-857-8
UNII:
4VDR6634UG
NSC Number:
5288
Properties
Computed Properties
 
Complexity:
55.4  
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:
1  
Topological Polar Surface Area:
20.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.9  

Synonyms
 
cyclohexanemethanol 
cyclohexylmethanol 
Benzyl alcohol, hexahydro- 
Cyclohexanemethanol, 99% - 25G 25g 
A15048 
100-51-6 
1015071-22-3 
101509-27-7 
89851-88-7 
USAF DO-49 
(Hydroxymethyl)cyclohexane 
Hydroxymethylcyclohexane 
NSC 5288 
Cyclohexyl methanol 
UNII-4VDR6634UG 
CyclohexYl-Methanol 
CYCLOHEXYL CARBINOL 
EINECS 202-857-8 
CYCLOHEXANEMETHANOL 
BRN 0773712 
AI3-01172 
4VDR6634UG 
VSSAZBXXNIABDN-UHFFFAOYSA-N 
MFCD00001510 
cyclohexylmethan-1-ol 
Cyclohexanemethanol, 99% 
cyclohexane-methanol 
PubChem3098 
hydroxymethyl-cyclohexane 
Cyclohexylmethanol 
ACMC-1BSUF 
4-cyclohexylmethylalcohol 
1-hydroxymethylcyclohexane 
(hydroxymethyl)-cyclohexane 
AC1L1OX1 
AC1Q7C8Z 
WLN: L6TJ A1Q 
SCHEMBL20903 
4-06-00-00106 (Beilstein Handbook Reference) 
AC1Q7C90 
100-49-2 
DTXSID3059212 
VSSAZBXXNIABDN-UHFFFAOYSA- 
NSC5288 
ACT10090 
BCP27207 
KS-000008VN 
NSC-5288 
ZINC1680819 
ANW-14298 
GEO-00862 
Cyclohexylcarbinol 
SBB061328 
AKOS000249005 
CS-W011242 
MCULE-6571547092 
NE10104 
RP19156 
TRA0041536 
TRA0084492 
AJ-29641 
AK-47687 
Cyclohexanecarbinol 
CJ-06285 
CJ-27629 
LS-56891 
M217 
SC-00039 
SY002783 
TS-01583 
DB-016119 
RT-000229 
AM20070443 
Hexahydrobenzyl alcohol 
FT-0624189 
ST24030281 
ST51047352 
Cyclohexanemethanol, ReagentPlus(R), >=99% 
EN300-21580 
MFCD00001510 (98%) 
65174-EP2269977A2 
65174-EP2277861A1 
65174-EP2298742A1 
65174-EP2308812A2 
Methanol, cyclohexyl- 
Cyclohexanemethanol, Vetec(TM) reagent grade, 98% 
I14-0566 
J-520159 
J-640289 
J-660045 
Z1201023032 
InChI=1/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2 
Cyclohexylmethanol, United States Pharmacopeia (USP) Reference Standard 
Cyclohexylmethane;cyclohexyl-methano;Cyclohexylmethyl alcohol;hexahydro-benzylalcohol 
benzyl alcohol 
Cyclohexylmethyl alcohol 
cyclohexylmethanol- 
cyclohexane methanol 
Cyclohexanemethanol- 
C7H14O 
Cyclohexanemethanol, 99% 25g 
CID7507 
C7-H14-O 
AR-1I3166 
c0595 
ACN-036583 
Literature

Title: Acceptorless photocatalytic dehydrogenation for alcohol decarbonylation and imine synthesis.

Journal: Angewandte Chemie (International ed. in English) 20120820

Title: Synthesis and structure of the β-carboline derivatives and their binding intensity with cyclin-dependent kinase 2.

Journal: Chemical & pharmaceutical bulletin 20120101

Title: Synthesis and evaluation of β-carboline derivatives as potential monoamine oxidase inhibitors.

Journal: Bioorganic & medicinal chemistry 20110101

Title: Design and synthesis of novel hydroxyalkylaminomethylchromones for their IL-5 inhibitory activity.

Journal: Bioorganic & medicinal chemistry 20100701

Title: Synthesis and evaluation of novel chromone analogs for their inhibitory activity against interleukin-5.

Journal: European journal of medicinal chemistry 20100601

Title: The role of alkoxy group on the A ring of isoflavones in the inhibition of interleukin-5.

Journal: Archives of pharmacal research 20070801

Title: Highly beta-selective O-glucosidation due to the restricted twist-boat conformation.

Journal: Organic letters 20070412

Title: Structural requirement of chalcones for the inhibitory activity of interleukin-5.

Journal: Bioorganic & medicinal chemistry 20070101

Title: The role of the hydrophobic group on ring A of chalcones in the inhibition of interleukin-5.

Journal: Archives of pharmacal research 20061101

Title: Surface induced hydrogen-bonded macrocluster formation of methanol on silica surfaces.

Journal: Langmuir : the ACS journal of surfaces and colloids 20051011

Title: Turbidity determination of the critical exponent eta in the liquid-liquid mixture methanol and cyclohexane.

Journal: The Journal of chemical physics 20040322

Title: Glimepiride pharmacokinetics in obese versus non-obese diabetic patients.

Journal: The Annals of pharmacotherapy 20040101

Title: Characterization of polychlorinated aromatic hydrocarbons by reversed-phase liquid chromatography with ultraviolet absorbance and mass spectrometric detection.

Journal: Journal of chromatography. A 20031017

Title: What controls the thickness of wetting layers near bulk criticality?

Journal: Physical review letters 20020826

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