2,5-Dimethyl-2,5-hexanediol supplier

Name
2,5-Dimethyl-2,5-hexanediol
EINECS 203-731-5
CAS No. 110-03-2
Article Data61
CAS DataBase
Density 0.939 g/cm³
Solubility soluble in water
Melting Point 86-90 °C
Formula C₈H₁₈O₂
Boiling Point 215.1 °C at 760 mmHg
Molecular Weight 146.23
Flash Point 126.7 °C
Transport Information
Appearance white crystalline flakes
Safety 22-24/25
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms 1,1,4,4-Tetramethyl-1,4-butanediol;2,5-Dihydroxy-2,5-dimethylhexane;NSC 5595;
PSA 40.46000
LogP 1.30840

Synthetic route

: 142-30-3
2,5-dihydroxy-2,5-dimethyl-3-hexyne

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With hydrogen; 0.25% Pd/Al2O3 In xylene at 80℃; under 22502.3 Torr; Product distribution / selectivity;	98.5%
With palladium on activated charcoal; hydrogen In ethyl acetate at 20℃; under 7500.75 Torr; for 12h; Autoclave;	84%
bei der katalytischen Hydrierung entstehen je nach den Bedingungen verschiedene Produkte.Hydrogenation;

: 6975-92-4
2,5-dimethyl-1-hexene

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With sodium tetrahydroborate; iron(II) phthalocyanine; dimethylsulfide; oxygen In ethanol at 20℃; under 760.051 Torr;	51%

: 3404-78-2
2,5-dimethylhex-2-ene

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With sodium tetrahydroborate; iron(II) phthalocyanine; dimethylsulfide; oxygen In ethanol at 20℃; under 760.051 Torr;	41%

: 75-65-0
tert-butyl alcohol

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With sulfuric acid; dihydrogen peroxide; iron(II) sulfate	36%
With sulfuric acid; dihydrogen peroxide; iron(II) sulfate
With mercury under 760 Torr; Heating; Irradiation; Yield given;
zinc sulfide In water for 4h; Irradiation;
With sulfuric acid; dihydrogen peroxide; iron(II) sulfate In water at 0 - 20℃; for 0.5h; pH=1; Dimerization;	0.130 mmol

: 54462-71-4
2,5-dibromo-2,5-dimethyl-hexane

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With water; potassium carbonate

: 917-64-6
methyl magnesium iodide

: 110-13-4
2,5-hexanedione

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
das Reaktionsprodukt liefert beim Zerlegen mit Wasser;

: 75-16-1
methylmagnesium bromide

: 110-13-4
2,5-hexanedione

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: methylmagnesium iodide

: 110-13-4
2,5-hexanedione

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 75-16-1
methylmagnesium bromide

: 539-88-8
4-oxopentanoic acid ethyl ester

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: methylmagnesium iodide

: 539-88-8
4-oxopentanoic acid ethyl ester

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: methyl magnesium (1+); bromide

: 539-88-8
4-oxopentanoic acid ethyl ester

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 917-64-6
methyl magnesium iodide

: 123-25-1
succinic acid diethyl ester

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: methylmagnesium iodide

: 123-25-1
succinic acid diethyl ester

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 142-30-3
2,5-dihydroxy-2,5-dimethyl-3-hexyne

A: 110-03-2
2,5-dimethyl-2,5-hexanediol

B: 3730-60-7
2,5-dimethylhexan-2-ol

Conditions

Conditions	Yield
bei der katalytischen Hydrierung entstehen je nach den Bedingungen verschiedene Produkte.Hydrogenation;
With hydrogen; platinum

: 927-81-1
trans-2,5-dimethyl-3-hexene-2,5-diol

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With hydrogen; palladium on activated charcoal In methanol

: 3730-60-7
2,5-dimethylhexan-2-ol

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With potassium permanganate In water
With 3,3-dimethyldioxirane In acetone for 24h; Ambient temperature;
With 3,3-dimethyldioxirane In acetone Rate constant; Ambient temperature; different solvents;
Multi-step reaction with 2 steps 1: aq. H2SO4, aq. H2O2 2: FeSO4*7H2O, aq. H2SO4 View Scheme

: 90951-87-4
2-Hydroperoxy-2,5-dimethylhexane

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With sulfuric acid; iron(II) sulfate

: 67-63-0
isopropyl alcohol

: 74-86-2
acetylene

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With acetone Irradiation;

: 592-13-2
2,5-dimethylhexane

A: 110-03-2
2,5-dimethyl-2,5-hexanediol

B: 3730-60-7
2,5-dimethylhexan-2-ol

Conditions

Conditions	Yield
With 4-nitroperbenzoic acid In chloroform at 60℃; for 36h; Yield given. Yields of byproduct given;
With 4-nitroperbenzoic acid In chloroform at 60℃; for 36h; Rate constant; proportion of velocity of the hydroxylation of tert- and sec. C-H-bonds;

: 110-13-4
2,5-hexanedione

: 74-88-4
methyl iodide

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
With magnesium In diethyl ether Ambient temperature;

: 75-65-0
tert-butyl alcohol

A: 110-03-2
2,5-dimethyl-2,5-hexanediol

B: 67-64-1
acetone

Conditions

Conditions	Yield
With hydrogen; Pt/titania In water for 10h; Ambient temperature; Irradiation;	A 0.018 mmol B 0.0016 mmol

: 75-65-0
tert-butyl alcohol

A: 110-03-2
2,5-dimethyl-2,5-hexanediol

B: 34557-54-5
methane

C: 67-64-1
acetone

D: 115-11-7
isobutene

Conditions

Conditions	Yield
With water G-values; Further Variations:; concentration; Decomposition; sonolysis;

...Expand

: 75-65-0
tert-butyl alcohol

A: 110-03-2
2,5-dimethyl-2,5-hexanediol

B: 558-42-9
3-chloro-2-methylpropan-2-ol

Conditions

Conditions	Yield
With dihydrogen peroxide; iron(II) chloride In water at 0 - 20℃; for 0.5h; pH=2; Dimerization; chlorination;	A 0.017 mmol B 0.127 mmol

: 7664-93-9
sulfuric acid

: 7722-84-1
dihydrogen peroxide

: iron(II) sulfate

: 75-65-0
tert-butyl alcohol

: 110-03-2
2,5-dimethyl-2,5-hexanediol

...Expand

: 539-88-8
4-oxopentanoic acid ethyl ester

methyl magnesium halide: methyl magnesium halide

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 7732-18-5
water

: 75-65-0
tert-butyl alcohol

hydrogen: hydrogen

oxygen: oxygen

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
Leiten einer wss.Loesung durch den inneren Kegel einer Wasserstoff-Sauerstoff-Flamme;

...Expand

: 75-65-0
tert-butyl alcohol

A: 75-85-4
tert-Amyl alcohol

B: 110-03-2
2,5-dimethyl-2,5-hexanediol

C: 34557-54-5
methane

D: 74-84-0
ethane

E: 67-64-1
acetone

F H2 (35.3 μ mol): H2 (35.3 μ mol)

Conditions

Conditions	Yield
Pt on TiO2 In water at 27℃; for 5h; Product distribution; Mechanism; Irradiation; reactions between var. conditions;	A 0.0074 mmol B 0.0159 mmol C 0.0121 mmol D 0.0013 mmol E 0.0151 mmol F n/a

...Expand

: 142-30-3
2,5-dihydroxy-2,5-dimethyl-3-hexyne

platinum: platinum

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
Hydrogenation;

: 67-56-1
methanol

: 142-30-3
2,5-dihydroxy-2,5-dimethyl-3-hexyne

Raney nickel: Raney nickel

: 110-03-2
2,5-dimethyl-2,5-hexanediol

Conditions

Conditions	Yield
at 25℃; under 147102 Torr; Hydrogenation;

...Expand

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 15045-43-9
2,2,5,5-tetramethyltetrahydrofuran

Conditions

Conditions	Yield
With beta-zeolite HCZB 25 at 0.85 - 105℃; for 1.5h; Reagent/catalyst;	100%
Nafion-H at 130℃; for 2h;	94%
With penthaethoxyphosphorane In dichloromethane for 450h; Ambient temperature;	79.1%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 6223-78-5
2,5-dichloro-2,5-dimethyl hexane

Conditions

Conditions	Yield
With hydrogenchloride In water	100%
With hydrogenchloride In water at 0℃; Inert atmosphere; Schlenk technique;	99%
With hydrogenchloride In water at 20℃; for 5.5h;	98%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 103603-61-8
2,5-dihypochloro-2,5-dimethylhexane

Conditions

Conditions	Yield
With sodium hypochlorite In tetrachloromethane; acetic acid	100%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

A: 123-56-8
Succinimide

B: 67-64-1
acetone

Conditions

Conditions	Yield
With N-iodo-succinimide In benzene for 0.916667h; Product distribution; Mechanism; Irradiation; varying reaction time;	A 88% B 99%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 71-43-2
benzene

: 6683-46-1
1,1,4,4-Tetramethyl-1,2,3,4-tetrahydro-naphthalene

Conditions

Conditions	Yield
With aluminium trichloride at 55℃; for 6h;	99%

: 546-68-9
titanium(IV) isopropylate

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: Ti(O(CH3)2CCH2CH2C(CH3)2O)(O(CH3)2CCH2CH2C(CH3)2OH)2

Conditions

Conditions	Yield
In benzene byproducts: isopropyl alcohol; to a benzene soln. of Ti(OPr-i)4 was added a soln. of glycol in benzene,the mixt. was refluxed for 12 h, cooled to room temp.; isopropanol was sepd. during the reaction azeotropically, the volatiles were removed at room temp. under reduced pressure, recrystd. from toluene-hexane at -20°C; elem. anal.;	99%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 103-71-9
phenyl isocyanate

: 1417339-50-4
2,5-dimethyl-2,5-bis-(N-phenylcarbamoyloxy)hexane

Conditions

Conditions	Yield
With MoCl2O2(dmf)2 In N,N-dimethyl-formamide at 60℃; for 0.5h; Inert atmosphere;	98%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 555-31-7
aluminum isopropoxide

: 54220-62-1
N-2,6-triethylphenylsalicylaldimine

: [OC(CH3)2CH2CH2C(CH3)2O]AlOC6H4CHNC6H3(C2H5)2

Conditions

Conditions	Yield
In benzene byproducts: i-PrOH; equimolar amounts of Al-comp., glycol and aldimine refluxed ca.24 h; solv. removed in vac., recrystd. from toluene/hexane 1:2 at -20°C, elem. anal.;	97%

...Expand

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 555-31-7
aluminum isopropoxide

: 54220-52-9
2-(((2,6-dimethylphenyl)imino)methyl)phenol

: [OC(CH3)2CH2CH2C(CH3)2O]AlOC6H4CHNC6H3(CH3)2

Conditions

Conditions	Yield
In benzene byproducts: i-PrOH; equimolar amounts of Al-comp., glycol and aldimine refluxed ca.24 h; solv. removed in vac., recrystd. from toluene/hexane 1:2 at -20°C, elem. anal.;	97%

...Expand

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 1609-86-5
Tert-butyl isocyanate

: 1417339-53-7
2,5-dimethyl-2,5-bis-(N-tert-butylcarbamoyloxy)hexane

Conditions

Conditions	Yield
With MoCl2O2(dmf)2 In dichloromethane for 4h; Inert atmosphere; Reflux;	94%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: (diethylamino)titanatrane

: 147244-59-5
2-(titanatranyloxy)-2,6-dimethyl-6-hydroxyhexane

Conditions

Conditions	Yield
In dichloromethane under Ar or N2, react. of (diethylamino)titanatrane and 2,5-dimethyl-2,5-hexandiol in equimolar amts., stirring for 1.5 h at room temp.; concg. under vac. to half volume, layering with pentane, cooling to -25°C, pptn. after 24 h;	92%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 51956-21-9
Mo2(O-t-Bu)6

: 1293913-57-1
[Mo2(OtBu)2(O2DMH)2]

Conditions

Conditions	Yield
In hexane byproducts: tBuOH; hexane soln. of ligand (0.64 mmol) added dropwise to hexane soln. of Mo compd. (0.32 mmol) at room temp., mixt. stirred for 3 h; filtered off, washed (hexane), recrystd. (CH2Cl2, -20°C), elem. anal.;	89%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 766-77-8
Dimethylphenylsilane

: 2,4,4,7,7-pentamethyl-2-phenyl-1,3,2-dioxasilepane

Conditions

Conditions	Yield
With sodium hydroxide In tetrahydrofuran; N,N-dimethyl-formamide at 60℃; for 24h; Sealed tube;	89%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 1631-84-1
dichlorophenylsilane

: 4,4,7,7-tetramethyl-2-phenyl-1,3,2-dioxasilepane

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 12h;	88%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 14717-56-7
zirconium(IV) tetraisopropoxide 2-propanol

: Zr(O(CH3)2CCH2CH2C(CH3)2O)(O(CH3)2CCH2CH2C(CH3)2OH)2

Conditions

Conditions	Yield
In benzene byproducts: isopropyl alcohol; to a benzene soln. of Zr(OPr-i)4 was added a soln. of glycol in benzene,the mixt. was refluxed for 12 h, cooled to room temp.; isopropanol was sepd. during the reaction azeotropically, the volatiles were removed at room temp. under reduced pressure, recrystd. from toluene-hexane at -20°C; elem. anal.;	87%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 630-19-3
pivalaldehyde

: 2-tert.-butyl-4,4,7,7-tetramethyl-1,3-dioxacycloheptane

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene	85%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 814-68-6
acryloyl chloride

: 3-(2,5-dimethylhexane-2,5-diyl)diacrylate

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 15h;	84%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: (diethylamino)titanatrane

: 2,6-bis(titanatranyloxy)-2,6-dimethylhexane

Conditions

Conditions	Yield
In dichloromethane under Ar or N2, react. of (diethylamino)titanatrane and 2,5-dimethyl-2,5-hexandiol in 2:1 molar ratio, stirring for 1.5 h at room temp.; concg. under vac. to half volume, layering with pentane, cooling to -25°C, pptn. after 24 h;	83%

: 5781-53-3
monomethyl oxalyl chloride

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 5-hydroxy-2,5-dimethylhexan-2-yl methyl oxalate

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;	81%
With dmap; triethylamine In dichloromethane at 0 - 20℃; for 12h; Inert atmosphere;	62%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 66012-50-8
1,5-bis(tetrazol-5-yl)-3-oxapentane

: 1412453-66-7
2,2,5,5-tetramethyl-12-oxa-1,6,7,8,16,17,18,19-octaaza-tricyclo-[13.2.1.16,9]nonadeca-7,9(19),15(18),16-tetraene

Conditions

Conditions	Yield
With perchloric acid In water at 20℃; for 72h;	80%
With perchloric acid In water at 20℃; for 72h; regioselective reaction;	80%

: 5781-53-3
monomethyl oxalyl chloride

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 2,5-dimethylhexane-2,5-diyl dimethyl dioxalate

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;	78%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 18039-42-4
5-phenyl-2H-1,2,3,4-tetrazole

: 2,5-dimethyl-2,5-di(5-phenyl-2-tetrazolyl)hexane

Conditions

Conditions	Yield
With perchloric acid at 20℃; for 2h; Alkylation;	76%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

A: 15045-43-9
2,2,5,5-tetramethyltetrahydrofuran

B: 14908-27-1
2,5-dimethyl-4-hexen-2-ol

Conditions

Conditions	Yield
With chloro-trimethyl-silane; dimethyl sulfoxide In benzene at 20℃; for 75h;	A 75% B 21%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 54935-70-5
hexakis(dimethylamido)ditungsten(III)

: 139728-87-3
W2(μ-2,5-dimethylhexane-2,5-diolate)(η(2)-2,5-dimethylhexane-2,5-diolate)2(dimethylamine)2

Conditions

Conditions	Yield
In tetrahydrofuran; hexane; toluene byproducts: HNMe2; N2-atmosphere; addn. of excess diol (in THF) to metal compd. (in hexane/PhMe=2:1 v/v) at -10°C, stirring at -10°C for 4 h; vol. reduction (vac.), crystn. (-20°C, 12 h), decantation, washing (cold hexane); elem. anal.;	75%
In diethyl ether; hexane -20°C, under N2; elem. anal.;

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 79-10-7
acrylic acid

: 3-(2,5-dimethylhexane-2,5-diyl)diacrylate

Conditions

Conditions	Yield
With N,N,N,N,-tetramethylethylenediamine; acetic anhydride at 60℃; for 5h; Cooling with ice;	75%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 140-29-4
phenylacetonitrile

A: 76528-08-0
5-Benzyl-4-isopropylidene-2,2-dimethyl-3,4-dihydro-2H-pyrrole

B: 76527-93-0
tetrahydrobenzindol

Conditions

Conditions	Yield
sulfuric acid at 0 - 20℃; for 4h;	A 15% B 72%

...Expand

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 51956-21-9
Mo2(O-t-Bu)6

: 188107-81-5
Mo2(μ-2,5-dimethylhexane-2,5-diolate)3

Conditions

Conditions	Yield
In tetrahydrofuran; hexane byproducts: t-BuOH; N2-atmosphere; dropwise addn. of 3 equiv. diol (in THF) to metal compd. (in hexane) over 5 min, stirring at room temp. for 2 d (pptn.); solvent removal (vac.), washing (Et2O at 0°C), dissoln. in PhMe at 60°C, crystn. (-20°C, overnight), collection (filtration), washing (hexane);	72%
In not given under N2; elem. anal.;

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: antimony isopropoxide

: 402789-89-3
Sb(OC(CH3)2CH2CH2C(CH3)2O)OC3H7

Conditions

Conditions	Yield
In benzene byproducts: isopropanol; the mixt. in benzene was refluxed fo 16 h; isopropanol was fractionated out azeotropically, the solvent was removedunder reduced pressure, distilled at 95°C/10 mm ; elem. anal.;	72%

: 110-03-2
2,5-dimethyl-2,5-hexanediol

: 86-73-7
9H-fluorene

: 77308-47-5
1,1,4,4-tetramethyl-2,2,3,3-tetrahydrobenzo[b]fluorene

Conditions

Conditions	Yield
aluminium trichloride In dichloromethane 0 deg C, 2 h, then rt, 24 h;	70%

2,5-Dimethyl-2,5-hexanediol Specification

The IUPAC name of 2,5-Dimethyl-2,5-hexanediol is 2,5-dimethylhexane-2,5-diol. With the CAS registry number 110-03-2, it is also named as 1,1,4,4-Tetramethyl-1,4-butanediol. The product's categories are Organic Building Blocks; Oxygen Compounds; Polyols. Besides, it is white crystalline flakes, which should be stored in a cool, ventilated warehouse. When you are using this chemical, please do not breathe dust. And you should avoid contact with skin and eyes. In addition, its molecular formula is C₈H₁₈O₂ and molecular weight is 146.23.

The other characteristics of this product can be summarized as: (1)EINECS: 203-731-5; (2)ACD/LogP: 0.37; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): 0.37; (5)ACD/LogD (pH 7.4): 0.37; (6)ACD/BCF (pH 5.5): 1.13; (7)ACD/BCF (pH 7.4): 1.13; (8)ACD/KOC (pH 5.5): 37.89; (9)ACD/KOC (pH 7.4): 37.89; (10)#H bond acceptors: 2; (11)#H bond donors: 2; (12)#Freely Rotating Bonds: 5; (13)Index of Refraction: 1.453; (14)Molar Refractivity: 42.11 cm³; (15)Molar Volume: 155.6 cm³; (16)Surface Tension: 33.3 dyne/cm; (17)Density: 0.939 g/cm³; (18)Flash Point: 126.7 °C; (19)Melting Point: 86-90 °C; (20)Enthalpy of Vaporization: 52.5 kJ/mol; (21)Boiling Point: 215.1 °C at 760 mmHg; (22)Vapour Pressure: 0.0328 mmHg at 25 °C.

Preparation of 2,5-Dimethyl-2,5-hexanediol: this chemical can be prepared by Acetylene and Acetone.

This reaction needs reagent by pressurizing ethynylation, condensation and hydrogenation. The reaction can be catalyzed by Raney nickel.

Uses of 2,5-Dimethyl-2,5-hexanediol: this chemical is used as an intermediate in organic synthesis. It can be used for the production of pyrethrins, spices, organic peroxide, artificial musk, crosslinker and polyether rubber. Moreover, it is used to produce 2,5-Dihypochloro-2,5-dimethylhexane.

This reaction needs 5percent Sodium hypochlorite, Acetic acid and CCl₄. The yield is 100 %.

People can use the following data to convert to the molecule structure.
(1)Canonical SMILES: CC(C)(CCC(C)(C)O)O
(2)InChI: InChI=1S/C8H18O2/c1-7(2,9)5-6-8(3,4)10/h9-10H,5-6H2,1-4H3
(3)InChIKey: ZWNMRZQYWRLGMM-UHFFFAOYSA-N

Product Name

2,5-Dimethyl-2,5-hexanediol

Synthetic route

2,5-Dimethyl-2,5-hexanediol Specification

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