methyl magnesium iodide
4c-hydroxy-4t-methyl-cyclohexane-r-carboxylic acid methyl ester
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
With emulsifierene; sulfuric acid |
ethanol
nitric acid
limonene.
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-limonene; |
Beta-pinene
sulfuric acid
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
Kinetics; levorotatory form; |
Beta-pinene
sulfuric acid
A
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
at 15 - 20℃; levorotatory form; |
ethanol
1-Chloro-4-(1-chloro-1-methyl-ethyl)-1-methyl-cyclohexane
water
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
'trans-form'; |
methanol
Pinene
nitric acid
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-pinene; |
Pinene
ethanol
nitric acid
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-pinene; |
Pinene
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-pinene; |
3,7-dimethyl-2E,6-octadien-1-yl acetate
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
at -5℃; |
linalool
sulfuric acid
A
Nerol
B
Geraniol
C
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Pinene
A
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
B
limonene.
Conditions | Yield |
---|---|
l-pinene; |
hydrogenchloride
terpineol
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-α-terpineol; |
terpineol
sulfuric acid
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
dl-α-terpineol; | |
at 0℃; dl-α-terpineol; |
sulfuric acid
trans-2,6,6-trimethylbicyclo(3.1.1)-heptan-2-ol
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
pinene hydrate; |
sulfuric acid
beta-terpineol
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
α-terpinyl chloride
water
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
d-limonene monohydrochloride; |
Conditions | Yield |
---|---|
Behandeln des Reaktionsprodukts mit Aether oder Sodaloesung; dl-α-terpineol; |
sulfuric acid
beta-pinene
A
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
at 0℃; |
Conditions | Yield |
---|---|
With chloroacetone | |
bei Einwirkung von Saeuren; |
Conditions | Yield |
---|---|
With phosphoric acid | |
With sulfuric acid |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
1-methyl-4-isopropyl-1,3-cyclohexadiene
Conditions | Yield |
---|---|
With phosphoric acid at 150 - 160℃; | |
With sulfuric acid | |
Multi-step reaction with 2 steps 1: concentrated hydrobromic acid 2: alcoholic sulfuric acid View Scheme | |
Multi-step reaction with 2 steps 1: bei der Einw. von wasserabspaltenden Mitteln 2: diluted sulfuric acid View Scheme |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
β-terpineol
Conditions | Yield |
---|---|
Dehydratisierung; |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
With phosphorus; hydrogen iodide at 210℃; |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
4-methylisopropylbenzene
Conditions | Yield |
---|---|
With Japanese Fuller's earth | |
With bromine |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
1-Chloro-4-(1-chloro-1-methyl-ethyl)-1-methyl-cyclohexane
Conditions | Yield |
---|---|
With hydrogenchloride 'trans-form'; | |
With hydrogenchloride; phosphorus trichloride 'trans-form'; | |
Multi-step reaction with 2 steps 1: bei der Einw. von wasserabspaltenden Mitteln 2: diethyl ether; hydrogen chloride View Scheme |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
1,8-dibromo-p-menthane
Conditions | Yield |
---|---|
With hydrogen bromide trans-form; | |
With hydrogen bromide cis-form; |
Conditions | Yield |
---|---|
With sulfuric acid dl-α-terpineol; | |
With oxalic acid dl-α-terpineol; | |
With sulfuric acid; benzene |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
A
terpineol
B
beta-terpineol
Conditions | Yield |
---|---|
bei der Einw. von wasserabspaltenden Mitteln; dl-α-terpineol; | |
With oxalic acid dl-α-terpineol; |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
A
terpineol
B
limonene.
Conditions | Yield |
---|---|
With Japanese acid earth at 200℃; bei der Destillation; dl-α-terpineol; |
Conditions | Yield |
---|---|
With sulfuric acid |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
beta-terpineol
Conditions | Yield |
---|---|
With sulfuric acid | |
bei der Einw. von wasserentziehenden Mitteln; |
cis-4-hydroxy-α,α,4-trimethyl-cyclohexanemethanol, monohydrate
Conditions | Yield |
---|---|
With carbon disulfide; phosphorous triiodide | |
With hydrogen iodide | |
Multi-step reaction with 2 steps 1: bei der Einw. von wasserabspaltenden Mitteln 2: hydrogen iodide View Scheme |
Conditions | Yield |
---|---|
With phosphoric acid at 200℃; | |
With potassium hydrogensulfate Abdestillieren des entstehenden Wassers; | |
With copper at 300℃; |
The Terpin hydrate is an organic compound with the formula C10H22O3. The IUPAC name of this chemical is 4-(2-hydroxypropan-2-yl)-1-methylcyclohexan-1-ol hydrate. With the CAS registry number 2451-01-6, it is also named as cis-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (1:1). The product's categories are Biochemistry; Monocyclic Monoterpenes; Terpenes. Besides, it should be stored in a closed cool and dry place.
Physical properties about Terpin hydrate are: (1)ACD/BCF (pH 5.5): 1; (2)ACD/BCF (pH 7.4): 1; (3)ACD/KOC (pH 5.5): 16.05; (4)ACD/KOC (pH 7.4): 16.05; (5)#H bond acceptors: 3; (6)#H bond donors: 4; (7)#Freely Rotating Bonds: 3; (8)Polar Surface Area: 40.46 Å2; (9)Flash Point: 156.8 °C; (10)Enthalpy of Vaporization: 67.06 kJ/mol; (11)Boiling Point: 335.7 °C at 760 mmHg; (12)Vapour Pressure: 8.16E-06 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, wear suitable gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: O.C[C@@]1(O)CC[C@@H](CC1)C(C)(C)O
(2)InChI: InChI=1/C10H20O2.H2O/c1-9(2,11)8-4-6-10(3,12)7-5-8;/h8,11-12H,4-7H2,1-3H3;1H2/t8-,10+;
(3)InChIKey: JGKJMBOJWVAMIJ-OFAZAQPOBP
(4)Std. InChI: InChI=1S/C10H20O2.H2O/c1-9(2,11)8-4-6-10(3,12)7-5-8;/h8,11-12H,4-7H2,1-3H3;1H2/t8-,10+;
(5)Std. InChIKey: JGKJMBOJWVAMIJ-OFAZAQPOSA-N
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