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Cyclohexanemethanol

  • CAS No.: 100-49-2
  • Purity: 99%
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1.What is the Cyclohexanemethanol ?

Cyclohexanemethanol (Cyclohexyl methanol) can be used as a starting material for the synthesis of cyclohexanecarboxaldehyde, cyclohexanecarboxylic acid, cyclohexanone, and 1,4-cyclohexadione by photocatalytic oxidation (PCO) using titanium dioxide nanoparticles as a catalyst.

isophthalic acid
121-91-5

isophthalic acid

cyclohexane-1,3-dicarboxylic acid
3971-31-1

cyclohexane-1,3-dicarboxylic acid

3-methylcyclohexanecarboxylic acid
13293-59-9

3-methylcyclohexanecarboxylic acid

cyclohexylmethyl alcohol
100-49-2

cyclohexylmethyl alcohol

Cyclohexanecarboxylic acid
98-89-5

Cyclohexanecarboxylic acid

Conditions
Conditions Yield
With 5% active carbon-supported ruthenium; hydrogen; In 1,4-dioxane; at 219.84 ℃; for 12h; under 51680.2 Torr;
methyl cyclohexylcarboxylate
4630-82-4

methyl cyclohexylcarboxylate

cyclohexylmethyl alcohol
100-49-2

cyclohexylmethyl alcohol

Conditions
Conditions Yield
With dimethylsulfide borane complex; In 2-methyltetrahydrofuran; at 90 ℃; for 0.333333h; under 7500.75 Torr; Inert atmosphere; Flow reactor;
95%
methyl cyclohexylcarboxylate; With 3-phenyl-propionaldehyde; diethylaluminum benzenethiolate; In hexane; toluene; at -78 ℃; for 1.08333h; Inert atmosphere;
With diisobutylaluminium hydride; In hexane; toluene; at -78 - 0 ℃; Inert atmosphere;
With hydrogenchloride; In hexane; water; toluene; at 0 ℃; chemoselective reaction;
93%
With C18H28Br2N4Ru; potassium tert-butylate; hydrogen; In 1,4-dioxane; at 105 ℃; for 8h; under 22502.3 Torr;
93%
With sodium tetrahydroborate; sodium methylate; In methanol; at 25 ℃; for 3h; Reagent/catalyst; Inert atmosphere;
90%
With hydrogen; sodium methylate; homogeneous ruthenium complex; In tetrahydrofuran; at 100 ℃; for 2.5h; under 37503.8 Torr;
89%
With phenylsilane; dimanganese decacarbonyl; In neat (no solvent); at 100 ℃; for 24h; Reagent/catalyst; Sealed tube;
85%
With hydrogen; sodium methylate; dichloro-bis-[2-(diphenylphosphino)ethylamine]ruthenium; In tetrahydrofuran; at 100 ℃; for 2.5h; under 37503.8 Torr; Product distribution / selectivity;
82%
With hydrogen; sodium methylate; trans, cis-[RuCl2(1-amino-2-diphenylphosphinoethane-N,P)2]; cis-RuCl2(Ph2P(CH2)2NH2)2; In tetrahydrofuran; at 100 ℃; for 2.5h; under 37503.8 Torr; Conversion of starting material;
82%
With n-butyllithium; [(1,2-bis[(2,6-diisopropylphenyl)imino]acenaphthene)FeCl2]; In hexane; toluene; at 100 ℃; for 20h; Inert atmosphere; Schlenk technique; Glovebox; Sealed tube;
82%
With tert-butyl alcohol; In tetrahydrofuran; electrolysis (Mg electrodes, LiClO4);
81%
With lithium aluminium tetrahydride; In diethyl ether; for 2h; Ambient temperature;
75%
With 15-crown-5; (1-(2-(2,3-diisopropyl-1-methylguanidino)ethyl)-3-mesityl-1,3-dihydro-2H-imidazol-2-ylidene)copper(I) chloride; hydrogen; sodium t-butanolate; In 1,4-dioxane; at 60 ℃; for 24h; Inert atmosphere;
54%
With [iPrPN(H)P]2Fe(H)(CO)(BH4); hydrogen; In toluene; at 115 ℃; for 24h; under 12654.8 Torr; Glovebox; Sealed tube;
50%
With zinc(II) tetrahydroborate; In 1,2-dimethoxyethane; for 24h; sonication; or with N,N-dimethylaniline, 14 h;
With titanium(IV) isopropylate; sodium hydroxide; Triethoxysilane; Yield given. Multistep reaction; 1.) heating, 16 h, 2.) THF, room temperature;
With hydrogen; sodium methylate; [RuCl2(R-BINAP)(S,S-DPEN)]; In tetrahydrofuran; at 60 ℃; for 16h; under 37503.8 Torr; Product distribution / selectivity;
51 %Chromat.
With Tridecane; hydrogen; sodium methylate; [((R,R)-diphenylethylenediamine)((R)-Binap)dichlororuthenium(II)]; In tetrahydrofuran; at 60 ℃; for 16h; under 37503.8 Torr; Autoclave;
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 45 ℃; for 1h;
methyl cyclohexylcarboxylate; With iron (II) stearate; ethylenediamine; In toluene; at 20 ℃; for 0.0833333h; Inert atmosphere; Schlenk technique;
In toluene; at 100 ℃; for 40h; Time; Inert atmosphere; Schlenk technique;
62 %Chromat.
With [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II); hydrogen; In tetrahydrofuran; at 120 ℃; for 19h; under 37503.8 Torr; Autoclave;
92 %Chromat.
With 1,1'-methylene-bis(3-benzyl-1H-imidazol-3-ium) diiodide; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; potassium tert-butylate; hydrogen; In 1,4-dioxane; at 100 ℃; for 6h; under 37503.8 Torr;
83 %Chromat.
With C27H31ClN4ORu; hydrogen; sodium t-butanolate; In toluene; at 105 ℃; for 20h; under 4500.45 Torr;
6 %Spectr.
With tris(triphenylphosphine)ruthenium(II) chloride; 2-diphenyl-1,2-ethylenediamine; potassium tert-butylate; hydrogen; In tetrahydrofuran; at 40 ℃; for 16h; Reagent/catalyst;
With diisobutylaluminium hydride; In diethyl ether; toluene; at -70 - 20 ℃;
With [{CyPN(H)P}Co(CH2SiMe3)]-BArF4; hydrogen; In tetrahydrofuran; at 120 ℃; for 20h; under 41254.1 Torr;
26 %Chromat.
With dichlorido-bis[(2-diphenylphosphino)ethyl]amine-cobalt(II); hydrogen; sodium methylate; In 1,4-dioxane; at 120 ℃; for 24h; under 37503.8 Torr; Autoclave;
52 %Chromat.
With HN(CH2CH2C3H3N2Mes)2Cl2; potassium tert-butylate; hydrogen; cobalt(II) chloride; In tetrahydrofuran; at 100 ℃; for 16h; under 22502.3 Torr; Autoclave; Glovebox;
80 %Chromat.
With potassium tert-butylate; hydrogen; In tetrahydrofuran; at 80 ℃; for 16h; under 37503.8 Torr; Autoclave; Glovebox;
With C36H62N2OP2Ru; hydrogen; In isopropyl alcohol; at 25 ℃; for 16h; under 22502.3 Torr; Autoclave;
98 %Chromat.
With C22H14MnN2O4(1+)*BF4(1-); potassium hydride; In tetrahydrofuran; at 50 ℃; Inert atmosphere; Glovebox; Sealed tube;

2.What is the CAS number for Cyclohexanemethanol ?

The CAS number of Cyclohexanemethanol is 100-49-2.

More information of Cyclohexanemethanol 100-49-2 are:

CAS?Number

100-49-2

Density

0.913 g/cm3

Melting Point

-43oC

Boiling Point

181.1 °C at 760 mmHg

Flash Point

71.1 °C

Vapor Pressure

0.254mmHg at 25°C

Refractive Index

n20/D 1.465(lit.)

HS CODE

29061900

PSA

20.23000

LogP

1.55900

Pka

15.17±0.10(Predicted)

3.What are another words for Cyclohexanemethanol ?

Synonyms?for?Cyclohexanemethanol 100-49-2:(Hydroxymethyl)cyclohexane;Cyclohexanecarbinol;Cyclohexylcarbinol;Cyclohexylmethylalcohol;NSC 5288;

4.What is the molecular formula of Cyclohexanemethanol?

The chemical formula of ?Cyclohexanemethanol is?C7H14O which containing 7 Carbon atoms,14 Hydrogen atoms and 1 Oxygen atoms,and the molecular weight of??Cyclohexanemethanol?is 114.188.

5.What is Cyclohexanemethanol (100-49-2) used for?

Cyclohexanemethanol, also known as Cyclohexyl methanol, is a colorless liquid with versatile applications across various industries. It is a valuable chemical intermediate and serves as a starting material for the synthesis of various compounds, including cyclohexanecarboxaldehyde, cyclohexanecarboxylic acid, cyclohexanone, and 1,4-cyclohexadione through photocatalytic oxidation (PCO) using titanium dioxide nanoparticles as a catalyst.

InChI:InChI=1/C7H14O/c8-6-7-4-2-1-3-5-7/h7-8H,1-6H2

Relevant articles related to Cyclohexanemethanol:

Article

Source

-

Rathke,Brown

, p. 2740 (1967)

Manganese-catalysed transfer hydrogenation of esters

Oates, Conor L.,Widegren, Magnus B.,Clarke, Matthew L.

, p. 8635 - 8638 (2020)

6.Buy Cyclohexanemethanol with the best price .

Hubei Yuancheng Saichuang Technology Co., Ltd is a quality supplier of Cyclohexanemethanol. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on Cyclohexanemethanol 100-49-2.

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