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1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol

  • CasNo:93413-76-4

Product Description

Quality products?make an important contribution to long-term revenue and profitability. 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol Good Manufacturer supply High Quality 93413-76-4

1.What is the 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol ?

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

1-[cyano(4-methoxyphenyl)methyl]cyclohexanol
93413-76-4,131801-69-9

1-[cyano(4-methoxyphenyl)methyl]cyclohexanol

Conditions
Conditions Yield
p-methoxybenzylnitrile; With sodium hydroxide; polyethylene glycol; In water; at 0 - 5 ℃; for 2h;
cyclohexanone; With sodium hydroxide; In water; at 0 - 20 ℃; for 13.5h;
90%
cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

p-methoxybenzylnitrile
104-47-2

p-methoxybenzylnitrile

1-[cyano(4-methoxyphenyl)methyl]cyclohexanol
93413-76-4,131801-69-9

1-[cyano(4-methoxyphenyl)methyl]cyclohexanol

Conditions
Conditions Yield
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In methanol; at 25 - 30 ℃; for 6h;
98%
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; at 0 - 15 ℃; for 1h;
97%
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In water; at 0 - 15 ℃; for 2.2h;
97.6%
With tetrabutylammomium bromide; sodium methylate; at 25 - 30 ℃; for 15h;
96%
With tetrabutylammomium bromide; water; sodium hydroxide; In methanol; at 20 ℃; for 15h;
96%
With ion-exchange resin IRA-900 (OH); at -60 ℃; for 100h; Flow reactor;
94%
With tetrabutylammomium bromide; sodium hydroxide; In toluene; at 50 ℃; for 5h; Reagent/catalyst; Solvent;
93.7%
p-methoxybenzylnitrile; With sodium methylate; In methanol; at 0 - 5 ℃; for 2h; Large scale reaction;
cyclohexanone; In methanol; at 0 - 5 ℃; for 4h; Large scale reaction;
91%
With tetrabutylammomium bromide; sodium hydroxide; In methanol; water; for 3h;
91.3%
With 1,8-diazabicyclo[5.4.0]undec-7-ene; potassium hydroxide; In methanol; water; at 15 - 20 ℃; for 24h;
90%
tetra-(n-butyl)ammonium iodide; In water; at 0 ℃; for 0.166667h;
89.7%
p-methoxybenzylnitrile; With n-butyllithium; In tetrahydrofuran; hexane; at -75 - -70 ℃; for 0.5h;
cyclohexanone; In tetrahydrofuran; hexane; at -70 - -65 ℃; for 4h;
With water; ammonium chloride; In tetrahydrofuran; hexane; at 0 ℃;
89%
potassium tert-butylate; In n-heptane; at 20 ℃; for 0.833333h; Product distribution / selectivity;
88.8%
cyclohexanone; p-methoxybenzylnitrile; potassium tert-butylate; In n-heptane; at 20 ℃; for 0.833333h;
With acetic acid; In n-heptane; Product distribution / selectivity;
88.8%
With sodium methylate; In methanol; at -5 - -2 ℃;
86.75%
p-methoxybenzylnitrile; With sodium methylate; In methanol; at 0 - 5 ℃; for 1.25 - 1.5h;
cyclohexanone; In methanol; at 0 - 5 ℃; for 3.5 - 4.16667h; Product distribution / selectivity;
85%
potassium tert-butylate; at 20 - 25 ℃; for 0.5h; Product distribution / selectivity;
82.4%
cyclohexanone; p-methoxybenzylnitrile; potassium tert-butylate; at 20 - 25 ℃; for 0.5h;
With acetic acid; In n-heptane; at 10 ℃; for 0.5h; pH=3 - 4; Product distribution / selectivity;
82.4%
p-methoxybenzylnitrile; With sodium methylate; In methanol; at -5 - -3 ℃; for 2h;
cyclohexanone; In methanol; at -5 - -3 ℃; for 10 - 12h;
With water; at 0 - 2 ℃; for 0.5h;
80%
p-methoxybenzylnitrile; With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -65 ℃; for 0.5h;
cyclohexanone; In tetrahydrofuran; at -78 - -65 ℃; for 2h;
80.7%
p-methoxybenzylnitrile; With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -65 ℃; for 0.5h;
cyclohexanone; In tetrahydrofuran; at -78 - -65 ℃; for 2h;
80.7%
p-methoxybenzylnitrile; With lithium diisopropyl amide; In tetrahydrofuran; at -78 - -65 ℃; for 0.5h;
cyclohexanone; In tetrahydrofuran; at -78 - -62 ℃; for 2h;
With water; ammonium chloride; In tetrahydrofuran; at 0 ℃; for 0.25h;
80.7%
With sodium hydroxide; In water; at 0 ℃; for 0.166667h;
78%
tetra(n-butyl)ammonium hydroxide; at 20 - 25 ℃; for 0.25h; Product distribution / selectivity;
73.6%
cyclohexanone; p-methoxybenzylnitrile; tetra(n-butyl)ammonium hydroxide; In water; at 20 - 25 ℃; for 0.25h;
With hydrogenchloride; In water; toluene; at 30 ℃; Product distribution / selectivity;
73.6%
potassium tert-butylate; In toluene; at 20 - 26 ℃; for 24h; Product distribution / selectivity;
68.2%
cyclohexanone; p-methoxybenzylnitrile; potassium tert-butylate; In toluene; at 20 - 26 ℃; for 24h;
With acetic acid; In n-heptane; at 10 ℃; for 0.5h; pH=3 - 4; Product distribution / selectivity;
68.2%
With n-butyllithium; Yield given. Multistep reaction; 1.) THF, hexane, -70 deg C, 30 min, 2.) -65 deg C, 2 h;
With sodium hydroxide; polyethyleneglycol monomethylether; In water; at 20 ℃; for 7 - 8h; Product distribution / selectivity;
With potassium hydroxide; polyethyleneglycol monomethylether; In water; at 5 - 25 ℃; for 5h; Product distribution / selectivity;
With potassium hydroxide; In polyethyleneglycol monomethyl ether; water; at 5 - 25 ℃; for 5h; Product distribution / selectivity;
With sodium hydroxide; In ethanol; water; at 25 ℃; for 4h; Product distribution / selectivity;
With sodium hydroxide; In ethanol; water; at 25 ℃; for 4h; Product distribution / selectivity;
With sodium hydroxide; In polyethyleneglycol monomethyl ether; water; at 20 ℃; for 7 - 8h; Product distribution / selectivity;
With sodium hydroxide; tetrabutylammomium bromide; In water; at 15 - 18 ℃; for 1.75h;
With sodium butanolate; In butan-1-ol; at -10 - -5 ℃; for 2.66667 - 2.83333h; Product distribution / selectivity;
With sodium t-butanolate; In tert-butyl alcohol; at -10 - -5 ℃; for 2.66667 - 2.83333h; Product distribution / selectivity;
With sodium isobutoxide; In 2-methyl-propan-1-ol; at -10 - -5 ℃; for 2.66667 - 2.83333h; Product distribution / selectivity;
p-methoxybenzylnitrile; With hexamethylenetetramine; potassium carbonate; In dimethyl sulfoxide; at 25 - 92 ℃; for 1 - 1.5h;
cyclohexanone; In dimethyl sulfoxide; at 20 ℃; for 1.5 - 2h;
p-methoxybenzylnitrile; With sodium methylate; In methanol; at -5 - -3 ℃; Inert atmosphere;
cyclohexanone; In methanol; at -5 - -3 ℃;
With water; In methanol; at 0 - 2 ℃; for 0.5h;
With sodium hydroxide; In methanol; water;
With pyridine; In tetrahydrofuran; at 45 - 65 ℃; Solvent; Reagent/catalyst; Temperature;
451.4 g
In ethanol; at 15 - 30 ℃; Alkaline conditions;

2.What is the CAS number for 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol ?

The CAS number of 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol is 93413-76-4.

More information of 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol 93413-76-4 are:

CAS?Number

93413-76-4

Density

1.142 g/cm3

Melting Point

121-123 °C

Boiling Point

410.146 °C at 760 mmHg

Flash Point

201.849 °C

Vapor Pressure

0mmHg at 25°C

Refractive Index

1.561

HS CODE

2926909090

PSA

53.25000

LogP

2.99758

Pka

13.80±0.20(Predicted)

3.What are another words for 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol ?

Synonyms?for?1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol 93413-76-4:1-[Cyano(4-methoxyphenyl)methyl]cyclohexanol;

4.What is the molecular formula of 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol?

The chemical formula of ?1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol is?C15H19NO2 which containing 15 Carbon atoms,19 Hydrogen atoms,1 Nitrogen atoms and 2 Oxygen atoms,and the molecular weight of??1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol?is 245.321.

5.What is 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol (93413-76-4) used for?

InChI:InChI=1/C15H19NO2/c1-18-13-7-5-12(6-8-13)14(11-16)15(17)9-3-2-4-10-15/h5-8,14,17H,2-4,9-10H2,1H3

Relevant articles related to 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol:

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6.Buy 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol with the best price .

Shanghai Huachu Industrial Co. Ltd is a quality supplier of 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol. Our main goal is customer satisfaction. Contact us to negotiate the best price for your business on 1-[Cyano-(p-methoxyphenyl)methyl]cyclohexanol 93413-76-4.

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