Appearance:white crystalline powder Storage:Stored in closed containers in dry cool conditions. Package:25kg/bag, Application:API Transportation:by air, by sea, by express
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inquiryProduct description: Product name Adamantane CAS number 281-23-2 Assay ≥99% Appearance White crystalline powder Capacity 500mt/year Application Pharmaceutical intermediates,
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inquiryItems Standard Result Appearance White crystalline powder Complies Assay 99.0%min
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inquiryAbout Product Details Item Specification Test Results Appearance White crystalline powder Conform
Cas:281-23-2
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【Chemical Name】Adamantane 【Synonym】Tricyclo[3.3.1.1(3,7)]decane 【CAS No】281-23-2 【Molecular Formula】C10H16 【Molecular Weight】136.26 【Structural Formula】 【Properties】White crystalline powder; Density: 1.07g/cm3(20/20 deg C); Melting Point: 266.00 -
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Conditions | Yield |
---|---|
With triethylsilane; dilauryl peroxide; 1-dodecylthiol at 70℃; for 1h; | 100% |
With triethylsilane; dilauryl peroxide; 1-dodecylthiol In cyclohexane at 80℃; for 1h; | 100% |
With sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); cPS-SnBu2Cl In 1,2-dimethoxyethane at 80℃; for 0.5h; | 100% |
1-adamantyl isocyanide
adamantane
Conditions | Yield |
---|---|
With Perbenzoic acid; diphenylsilane In 1,4-dioxane for 1h; Heating; | 100% |
1-(phenylseleno)tricyclo<3.3.1.13,7>decane
adamantane
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); 1,1,2,2-tetraphenyldisilane In ethyl acetate for 14h; Reduction; Heating; | 100% |
With Perbenzoic acid; methyl phosphite In 1,4-dioxane for 5h; Heating; | 41 % Chromat. |
O-(adamantan-1-yl) S-methyl carbonodithioate
adamantane
Conditions | Yield |
---|---|
With sodium formate; (Bu4N)2S2O8 In N,N-dimethyl-formamide at 75℃; for 0.5h; Barton-McCombie deoxygenation; | 100% |
With 2,2'-azobis(isobutyronitrile); tris-(trimethylsilyl)silane In toluene at 130℃; for 0.0833333h; Barton-McCombie deoxygenation; | 77% |
With 1-ethyl-piperidine; 2,2'-azobis(isobutyronitrile); hypophosphorous acid In 1,4-dioxane for 1h; | 100 % Chromat. |
With dibutylphosphine oxide; 1,1'-azobis(1-cyanocyclohexanenitrile) In 1,4-dioxane for 8h; Heating; | 90 % Chromat. |
Conditions | Yield |
---|---|
With triisopropylborane; trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane 1.) -30 deg C, 30 min 2.) room temp., 6 h; | A 99.9% B 0.1% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 180℃; | 99% |
With indium(III) chloride; diphenylsilyl chloride In 1,2-dichloro-ethane at 80℃; for 3h; | 99% |
With boron trifluoride diethyl etherate In water for 2h; Inert atmosphere; Reflux; | 29% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 170℃; | 99% |
Multi-step reaction with 2 steps 1: 81 percent / NaI; HI / 48 h / 90 - 100 °C 2: 35 percent Chromat. / t-BuOK / dimethylsulfoxide / 3 h / Irradiation View Scheme | |
Multi-step reaction with 2 steps 1: 81 percent / NaI; HI / 48 h / 90 - 100 °C 2: 20 percent Chromat. / t-BuOK / dimethylsulfoxide / 3 h / Irradiation View Scheme |
Conditions | Yield |
---|---|
With tris(trifluoromethanesulfonyloxy)boron In 1,1,2-Trichloro-1,2,2-trifluoroethane at 0 - 20℃; for 0.5h; | 98% |
With tris(trifluoromethanesulfonyloxy)boron In 1,1,2-Trichloro-1,2,2-trifluoroethane at 0 - 20℃; for 0.5h; Product distribution; sonication, other C(4n+6)H(4n+12), (n=1-3), other polycyclic hydrocarbon, other reactants, reaction condition; | 98% |
With aluminium trichloride at 150 - 180℃; | |
Mechanism; application of the "prinzip of minimal chemical distance"; |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); (C6F13CH2CH2)3SnH; sodium cyanoborohydride In tert-butyl alcohol at 90℃; for 3h; | 98% |
With air; tributyl borane; water In benzene at 20℃; | 97% |
With 1,3-bis(2,6-diiopropylphenyl)imidazol-2-ylidene borane In 1,2,3-trifluorobenzene at 140℃; for 12h; | 97% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tributyltin chloride; sodium cyanoborohydride; oxygen-18 In tert-butyl alcohol at 60℃; for 16h; Yields of byproduct given; | A n/a B 98% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 235℃; under 760 Torr; for 4h; | 97% |
Octahydro-1,2,4-metheno-1H-cyclobutapentalene
adamantane
Conditions | Yield |
---|---|
With sodium tetrahydroborate; trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane at -78 - 20℃; for 18h; | 97% |
1-acetyloxyadamantane
adamantane
Conditions | Yield |
---|---|
With hafnium(IV) trifluoromethanesulfonate; palladium 10% on activated carbon; hydrogen In neat (no solvent) at 125℃; under 750.075 Torr; for 18h; Time; | 97% |
With di-tert-butyl peroxide; (4-diphenylsilylphenyl)diphenylsilane at 140℃; for 15h; | 85% |
Conditions | Yield |
---|---|
With sulfuric acid In ethanol; water for 44h; Heating; | 97% |
Conditions | Yield |
---|---|
With triethylsilane; 2C2H3F3O*BF3 In dichloromethane at 20℃; for 3h; | 97% |
With gallium(III) triflate; dimethylmonochlorosilane In dichloromethane at 20℃; for 0.5h; | 88% |
With triethylsilane; 2C24BF20(1-)*C21H16N3P(2+) In dichloromethane at 120℃; for 13h; Inert atmosphere; | 94 %Spectr. |
1-Adamantyl bromide
trimethylstannane
A
adamantane
B
n-butyltrimethyltin
Conditions | Yield |
---|---|
With n-butyllithium In hexane 1-bromoadamantane (1 equiv.) and TMTH (1 equiv.) in hexane cooled to 0°C under Ar, n-BuLi (1 equiv., 2.40 M in hexane) added, stirred for 15 min, quenched with water; analyzed by GC; | A 97% B 95% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 200℃; | 96% |
With cerium(III) chloride; 9,10-diphenylanthracene; 1,2-bis(2,4,6-triisopropylphenyl)disulfane; tetrabutyl-ammonium chloride In acetonitrile for 24h; Irradiation; Inert atmosphere; | 95% |
bi(cyclopentadiene)
adamantane
Conditions | Yield |
---|---|
With sodium tetrahydroborate; trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane at -78 - 20℃; for 18h; | 96% |
With sodium tetrahydroborate; trifluoric acid In 1,1,2-Trichloro-1,2,2-trifluoroethane at -78 - 20℃; for 18h; Product distribution; other unsaturated polycyclics; | 96% |
1-(adamantane-1-carbonyloxy)pyridine-2(1H)-thione
adamantane
Conditions | Yield |
---|---|
With 9-borabicyclo[3.3.1]nonane dimer; tri-n-butyl-tin hydride In toluene at 0℃; | 96% |
With thiophenol In tetrahydrofuran at -80℃; Product distribution; Mechanism; Irradiation; | |
With 2,2'-azobis(isobutyronitrile); Tris(trimethylsilyl)methane In benzene at 80℃; | 89 % Chromat. |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); oxygen; tert-butyldibutyltin chloride; sodium cyanoborohydride In tert-butyl alcohol at 60℃; for 20h; Yields of byproduct given; | A n/a B 96% |
With 2-(2-methoxyethoxy)ethyl alcohol; oxygen; sodium hydride In 1,4-dioxane at 20℃; for 24h; Schlenk technique; chemoselective reaction; | A 42% B n/a |
Conditions | Yield |
---|---|
With [2-(di-tert-butylphosphinomethyl)-6-(diethylaminomethyl)pyridine]ruthenium(II) chlorocarbonyl hydride; isopropyl alcohol; sodium t-butanolate at 100℃; for 18h; Inert atmosphere; Sealed tube; Green chemistry; | 95% |
With air; diethylzinc; tri-n-butyl-tin hydride In benzene at 20℃; for 1h; | 90% |
With water; zinc In acetonitrile at 80℃; for 41h; Inert atmosphere; Sealed tube; | 53% |
octahydro-4,7-methano-inden-5-one
adamantane
Conditions | Yield |
---|---|
With sodium tetrahydroborate; trifluorormethanesulfonic acid In 1,1,2-Trichloro-1,2,2-trifluoroethane at -78 - 20℃; for 18h; | 95% |
Conditions | Yield |
---|---|
With hydrogen; aluminum oxide; nickel at 180℃; Pd/SiO2, 330 deg C; | 95% |
Multi-step reaction with 2 steps 1: DCC, DMAP 2: 93 percent / Bu3SnH, AIBN / benzene / 3 h / Heating View Scheme | |
Multi-step reaction with 2 steps 1: 28 percent / 85percent H2O2 2: 3 percent Chromat. / cyclohexane / 81 °C View Scheme |
1,3-dichloroadamantane
adamantane
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium; N,N-diethyl-1,1,1-trimethylsilanamine In diethyl ether for 6h; Ambient temperature; | 95% |
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In acetonitrile at 20℃; Irradiation; | A 3% B n/a C 95% |
C24H25NO2Se
adamantane
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride In benzene for 3h; Heating; | 93% |
adamantane-1-carboxylate
adamantane
Conditions | Yield |
---|---|
With triethylsilane; C19H3BF14 In dichloromethane at 20℃; Inert atmosphere; Schlenk technique; | 93% |
ethyl dispiro[1,3-dithiolane-2',2;4',2''-bis(adamantane)]-5'-carboxylate
A
adamantane
B
(2-Adamantyl)essigsaeure-ethylester
Conditions | Yield |
---|---|
nickel In methanol | A n/a B 92% |
Conditions | Yield |
---|---|
With zirconocene dichloride; triethyl borane In tetrahydrofuran; hexane at 25℃; for 5h; | 92% |
With iron(III) chloride; phenylsilane; sodium methylate In tetrahydrofuran for 12h; Schlenk technique; Inert atmosphere; | 89% |
With Schwartz's reagent; triethyl borane In tetrahydrofuran at 25℃; for 17h; | 88% |
Conditions | Yield |
---|---|
With azobisisobutyronitrile; sodium cyanoborohydride In α,α,α-trifluorotoluene; tert-butyl alcohol | 92% |
With azobisisobutyronitrile; sodium cyanoborohydride In α,α,α-trifluorotoluene; tert-butyl alcohol | 92% |
Conditions | Yield |
---|---|
In water-d2; d(4)-methanol at 19.84℃; for 0.0833333h; | 100% |
Conditions | Yield |
---|---|
With iron(III)-acetylacetonate; carbon tetrabromide Reagent/catalyst; Sealed tube; Inert atmosphere; | A 99% B 23% |
With bromine; iron at 0 - 50℃; for 3h; | A n/a B 93% |
With iodine(I) bromide In tetrachloromethane for 3h; Heating; | A 75 % Chromat. B 25 % Chromat. |
With iodine(I) bromide In tetrachloromethane for 3h; Heating; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With Fe(AAEMA)3; oxygen; isovaleraldehyde In 1,2-dichloro-ethane under 760 Torr; for 60h; Ambient temperature; | 99% |
With oxone; 1,1,1-trifluoro-2-propanone; sodium hydrogencarbonate In dichloromethane; water at 0 - 25℃; under 3878.71 Torr; for 0.0222222h; Reagent/catalyst; Temperature; Solvent; | 99% |
With water; bromine for 1h; Ambient temperature; | 95% |
adamantane
1-(1-adamantyl)chlorophosphinoyladamantane
Conditions | Yield |
---|---|
With aluminum (III) chloride; phosphorus trichloride for 6.16667h; Reflux; | 99% |
Stage #1: adamantane With aluminum (III) chloride; phosphorus trichloride Reflux; Stage #2: With water Cooling with ice; | 99% |
With aluminium trichloride; phosphorus trichloride for 5h; Heating; | 95% |
With aluminium trichloride; phosphorus trichloride for 5h; Heating; | 86.2% |
With aluminium trichloride; water; phosphorus trichloride 1.) reflux, 6 h, 2.) chloroform; Yield given. Multistep reaction; |
adamantane
adamantane-d16
Conditions | Yield |
---|---|
With d8-isopropanol; 5% rhodium-on-charcoal; 10% Pt/activated carbon; water-d2 at 120℃; for 24h; Sealed tube; | 99% |
Conditions | Yield |
---|---|
With bromine; Nitrogen dioxide In trifluoroacetic acid at 20℃; for 0.5h; | 98% |
With water; bromine for 0.166667h; | 93% |
With bromine at 85 - 110℃; Temperature; | 93% |
adamantane
1,3-dichloroadamantane
Conditions | Yield |
---|---|
With Iodine monochloride In tetrachloromethane for 5h; Heating; | 98% |
With chlorosulfonic acid at 0 - 25℃; for 10h; | 98% |
With chlorosulfonic acid at 0 - 25℃; for 8h; | 98% |
Conditions | Yield |
---|---|
With oxone; 1,1,1-trifluoro-2-propanone; sodium hydrogencarbonate In dichloromethane; water at 0 - 25℃; under 3878.71 Torr; for 0.0222222h; | 98% |
With potassium sulfate; sulfuric acid at 40 - 55℃; for 40h; Product distribution / selectivity; | 87% |
With lithium sulfate; sulfuric acid at 40 - 55℃; for 40h; Product distribution / selectivity; | 87% |
Conditions | Yield |
---|---|
With tetrachloromethane; manganese(III) acetylacetonate; acetonitrile at 200℃; for 1h; | 98% |
With Iodine monochloride In tetrachloromethane for 0.25h; Ambient temperature; | 97% |
With tetrachloromethane; ferrocene; ethanol at 160℃; for 6h; Sealed tube; | 93% |
Conditions | Yield |
---|---|
With tetrachloromethane; K10 bentonite; iron(III) chloride for 40h; Heating; | A 2% B 98% |
With tetrachloromethane; bis(acetylacetonate)oxovanadium; water at 160℃; for 6h; Sealed tube; | A 90% B n/a |
With thionyl chloride; n-Butyl chloride; sulfuric acid at 30℃; for 30h; | A 73% B 10.5% |
adamantane
1,3,5,7-tetrachloroadamanatane
Conditions | Yield |
---|---|
With tetrachloromethane; aluminium trichloride for 1h; Heating; | 98% |
With aluminum (III) chloride In tetrachloromethane Reflux; | 91% |
Conditions | Yield |
---|---|
With Rh(PPh3)3Cl In dichloromethane at 150℃; for 3h; | 98% |
Conditions | Yield |
---|---|
With bromine; iron In 1,1,2-Trichloro-1,2,2-trifluoroethane at 30℃; for 8h; | 97.3% |
With bromine; iron at 20℃; for 2h; Cooling with ice; | 96% |
With bromine at 0 - 25℃; | 85% |
Conditions | Yield |
---|---|
With nitrosonium tetrafluoroborate for 4h; reflux; | 97% |
With sulfuric acid at 3 - 25℃; for 5h; | 97% |
With bromine for 0.666667h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; Ba; trifluoroacetic acid In dichloromethane at 20℃; for 0.0333333h; Product distribution; | A n/a B 97% C n/a |
With [2,2]bipyridinyl; Ba; trifluoroacetic acid In dichloromethane at 20℃; for 0.0333333h; Yields of byproduct given; | A n/a B 97% C n/a |
With ammonium cerium(IV) nitrate; oxygen In acetonitrile for 5h; Ambient temperature; Irradiation; | A 5% B 85% C 5% |
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