cas 71-23-8 Name 1-Propanol Appearance colorless liquid Application Pharmaceutical Intermediates Appearance: Colorless liquid Storage:Preserve in w
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Cas:71-23-8
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inquiryProduct Description Product website: http://www.finerchem.com Product Name 1-Propanol CAS No. 71-23-8
Cas:71-23-8
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1-Propanol CAS RN.: 71-23-8 EINECS: 200-746-9 Molecular Weight: 60.1 Molecular Formula: C3H8O Density: 0.8 Melting Point(℃):
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Product Name: 1-Propanol Synonyms: n-PROPYL ALCOHOL, REAGENT (ACS)n-PROPYL ALCOHOL, REAGENT (ACS)n-PROPYL ALCOHOL, REAGENT (ACS);Natural Propanol;alcoolpropilico;alcoolpropylique;alcoolpropylique(french);caswellno709a;epapesticidechemicalcode04750
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A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Cas:71-23-8
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Cas:71-23-8
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
Conditions | Yield |
---|---|
With hydrogen; mer-Os(PPh3)3HBr(CO) at 150℃; under 22800 Torr; for 1.66667h; Product distribution; | 100% |
With hydrogen; mer-Os(PPh3)3HBr(CO) In toluene at 150℃; under 22800 Torr; for 1.7h; | 100% |
With hydrogen In water at 60℃; under 15001.5 Torr; for 8h; Reagent/catalyst; Autoclave; | 100% |
Conditions | Yield |
---|---|
With hydrogen; poly-1,2,3-triazolyl ferrocenyl dendrimer-Pd nanoparticle In methanol; chloroform at 25℃; under 760.051 Torr; | 100% |
With (1+)*OTf(1-); Gantrez 149; bis[(2-diphenylphosphino)ethyl]amine hydrochloride; hydrogen at 25℃; Mechanism; Product distribution; 1.) CH3CN, 10 h; 2.) H2O; var. Rh(I) complex cat., solvent; | 95% |
With <(Pd5Phen2)OAc>n; hydrogen In water at 30℃; Product distribution; hydogen and substrate concentration dependence; | 90% |
Conditions | Yield |
---|---|
With C61H62ClN3P2Ru In dichloromethane-d2 at 50℃; under 3040.2 Torr; for 10h; Reagent/catalyst; Time; | 100% |
dimethyl cis-but-2-ene-1,4-dioate
A
tetrahydrofuran
B
2-methoxytetrahydrofuran
C
4-butanolide
D
propan-1-ol
E
2-(4'-hydroxybutoxy)-tetrahydrofuran
F
Butane-1,4-diol
G
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; copper catalyst, T 4489, Sud-Chemie AG, Munich at 150 - 280℃; under 187519 Torr; Neat liquid(s) and gas(es)/vapour(s); | A 1% B n/a C 0.4% D n/a E n/a F 98% G 0.5% |
Conditions | Yield |
---|---|
With hydrogen In water at 119.84℃; under 60006 Torr; for 2h; Catalytic behavior; Reagent/catalyst; Autoclave; Sealed tube; | 97% |
propionic acid
propan-1-ol
Conditions | Yield |
---|---|
Stage #1: propionic acid With borane-2-methyltetrahydrofuran complex In 2-methyltetrahydrofuran at 0 - 20℃; for 2h; Stage #2: With water In 2-methyltetrahydrofuran Product distribution / selectivity; | 96.5% |
With hydrogen In water at 119.84℃; under 7500.75 - 60006 Torr; for 2h; Catalytic behavior; Reagent/catalyst; Autoclave; Sealed tube; | 96% |
With hydrogen In water at 100℃; under 37503.8 Torr; for 12h; Pressure; Reagent/catalyst; Autoclave; | 94% |
Conditions | Yield |
---|---|
With [C6H3-2,6-(OP(tBu)2)2]IrH2; trifluorormethanesulfonic acid; water; hydrogen In 1,4-dioxane at 125℃; under 5171.62 Torr; Temperature; Pressure; Solvent; Autoclave; | 95% |
With hydrogen In water at 210℃; under 30753.1 Torr; for 5h; Autoclave; Sealed tube; | |
With hydrogen In water at 179.84℃; under 37503.8 Torr; for 12h; | 80 %Chromat. |
at 315℃; Gas phase; |
propan-1-ol
Conditions | Yield |
---|---|
With N-ethyl-N-hydroxy-ethanamine; sodium hydroxide In tert-butyl alcohol for 2h; | 93% |
dipropyl phenylarsonate
benzyl bromide
A
propan-1-ol
B
propyl bromide
C
C16H19AsO3
Conditions | Yield |
---|---|
at 150℃; for 1.5h; | A n/a B n/a C 91.7% |
Conditions | Yield |
---|---|
With hydrogen at 180℃; under 37503.8 Torr; Catalytic behavior; chemoselective reaction; | A 91.2% B 7.8% |
With hydrogen In water at 179.84℃; under 22502.3 Torr; for 10h; Autoclave; | A 76% B 9% |
With hydrogen In water at 130℃; under 30003 Torr; for 24h; |
Conditions | Yield |
---|---|
In ethanol at 180℃; under 3750.38 Torr; for 24h; Inert atmosphere; Autoclave; | A 6% B 90% |
With hydrogen at 210℃; under 33753.4 Torr; for 12h; Catalytic behavior; Reagent/catalyst; Temperature; Pressure; | A n/a B 51.3% |
With hydrogen In 1,4-dioxane at 139.84℃; under 60006 Torr; for 24h; | A 34% B 18% |
Conditions | Yield |
---|---|
With (Ppyz)Zr(BH4)2Cl2 In diethyl ether for 4h; Heating; | 90% |
With isobutylmagnesium bromide; bis(cyclopentadienyl)titanium dichloride In diethyl ether for 1h; Ambient temperature; Yield given; | |
With hydrogen In water at 179.84℃; under 37503.8 Torr; for 6h; | |
With hydrogen In water at 150℃; under 37503.8 Torr; for 16h; Autoclave; | > 99 %Chromat. |
tripropyl arsenite
benzene-1,2-diol
A
propan-1-ol
B
o-hydroxyphenylenoxybenzo-1,3,2-dioxaarsole
Conditions | Yield |
---|---|
at 145 - 155℃; | A n/a B 90% |
Conditions | Yield |
---|---|
palladium anchored polystyrene In neat (no solvent) at 25℃; under 41371.8 Torr; for 15h; | A 5% B 90% |
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A n/a B 85% |
With hydrogen; palladium dichloride In N,N-dimethyl-formamide under 18751.5 Torr; for 0.316667h; Product distribution; Ambient temperature; various time; | A 2.6% B 76.3% |
propylamine
benzaldehyde
acetophenone
A
propan-1-ol
B
2,4,6-triphenylpyridine
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate at 120℃; for 4.5h; Neat (no solvent); regioselective reaction; | A 85 %Chromat. B 89% |
methyl crotonate
propan-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate; C36H30F6N10Ni4O10(2+)*2C2F3O2(1-); zinc(II) chloride In tetrahydrofuran at 45℃; for 12h; | 89% |
chloral hydrate
phenyl phosphinic acid dipropyl ester
A
propan-1-ol
B
C11H14Cl3O3P
Conditions | Yield |
---|---|
In benzene at 30 - 40℃; Abramov reaction; Inert atmosphere; | A n/a B 88% |
Conditions | Yield |
---|---|
With hydrogen In 1,4-dioxane at 159.84℃; under 60006 Torr; for 24h; Autoclave; | A 87% B 9% |
With [Ru(OH2)3(4'-phenyl-2,2':6',2''-terpy)](OTf)2; hydrogen; ortho-tungstic acid In water at 250℃; under 41254.1 Torr; for 24h; | A 39 %Chromat. B 52 %Chromat. |
With hydrogen In water at 200℃; under 18751.9 Torr; for 16h; Autoclave; |
Conditions | Yield |
---|---|
With hydrogen In water at 100℃; under 37503.8 Torr; for 30h; Pressure; Reagent/catalyst; Autoclave; | A 10% B 85% |
Conditions | Yield |
---|---|
In isopropyl alcohol at 180℃; under 3750.38 Torr; for 12h; Inert atmosphere; Autoclave; | A 6% B 84% C 6% |
With hydrogen In water at 200℃; under 60006 Torr; for 18h; Reagent/catalyst; Autoclave; | |
With iridium on carbon; hydrogen In water at 200℃; under 37503.8 Torr; for 4h; | |
With hydrogen In water at 200℃; under 18617.8 Torr; for 12h; Catalytic behavior; Reagent/catalyst; Autoclave; | |
With hydrogen In water at 220℃; under 60006 Torr; for 120h; Catalytic behavior; Reagent/catalyst; Autoclave; |
4-benzyloxycarbonylaminobutyric acid propyl ester
A
propan-1-ol
B
4-(benzyloxycarbonylamino)butyric acid
Conditions | Yield |
---|---|
With methanol; Bacillus subtilis esterase In hexane at 37℃; for 0.5h; pH=7.4; Kinetics; Reagent/catalyst; Time; aq. phosphate buffer; Enzymatic reaction; | A n/a B 83% |
4-butanolide
A
tetrahydrofuran
B
propan-1-ol
C
Butane-1,4-diol
D
butyric acid
E
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen; 5% platinum on alumina at 250℃; under 152000 Torr; Product distribution; var. catalysts; | A 82.3% B 1% C 4.8% D 1.2% E 1% |
2,2-pentamethylene-3-(trimethylsilyl)-5-propyl-2,5-dihydrofuran
A
propan-1-ol
B
5,5-pentamethylene-4-(trimethylsilyl)-2(5H)-furanone
Conditions | Yield |
---|---|
With oxygen for 72h; Ambient temperature; | A n/a B 82% |
dimethyl cis-but-2-ene-1,4-dioate
A
tetrahydrofuran
B
2-methoxytetrahydrofuran
C
4-butanolide
D
propan-1-ol
F
2-(4'-hydroxybutoxy)-tetrahydrofuran
H
Butane-1,4-diol
I
4-hydroxybutyraldehyde
J
methyl 4-hydroxybutanoate
K
butan-1-ol
Conditions | Yield |
---|---|
With hydrogen at 190℃; under 46504.7 Torr; Gas phase; | A 5.3% B n/a C 10.4% D n/a E n/a F n/a G n/a H 79.1% I n/a J n/a K n/a |
Conditions | Yield |
---|---|
With ruthenium-carbon composite; hydrogen In water at 119.84℃; under 7500.75 - 60006 Torr; for 2h; Catalytic behavior; Autoclave; Sealed tube; | A 18% B 79% |
Conditions | Yield |
---|---|
With ZnCuO2; hydrogen at 260℃; under 750.075 Torr; | A 77.2% B 6.7% C 5.3% |
Conditions | Yield |
---|---|
N2 or Ar atmosphere or vac.; stirring (50°C); | A 19% B 76% C 77% |
Conditions | Yield |
---|---|
With C18H28Br2N4Ru; potassium tert-butylate; hydrogen In 1,4-dioxane at 105℃; under 22502.3 Torr; for 8h; | 77% |
Stage #1: propyl propionate With iron (II) stearate; ethylenediamine In toluene at 20℃; for 0.0833333h; Inert atmosphere; Schlenk technique; Stage #2: In toluene at 100℃; for 20h; Inert atmosphere; Schlenk technique; | 75 %Chromat. |
With [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II); hydrogen In tetrahydrofuran at 120℃; under 22502.3 Torr; for 19h; Autoclave; | 68 %Chromat. |
propan-1-ol
propene
Conditions | Yield |
---|---|
With mesoporous silica MCM-4l/Al at 349.84℃; for 50h; | 100% |
aluminum oxide at 375℃; under 6000.6 Torr; | 99% |
With HZSM-5zeolite with a SiO2/Al2O3 at 250℃; Reagent/catalyst; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With oxygen; phosphan; copper dichloride at 24.9℃; Rate constant; Product distribution; other acohols and reagents, var. concentration of reagents and temperatures; | 100% |
With oxygen; phosphan; copper dichloride at 24.9℃; | 100% |
With trichlorophosphate In acetone at 10 - 30℃; under 10 Torr; for 4h; | 97% |
propan-1-ol
propionic acid
Conditions | Yield |
---|---|
With ammonium cerium (IV) nitrate; sodium trimethylsilylpropionate-d4; C18H22N4O2Ru(2+)*2F6P(1-); water at 20℃; for 0.5h; | 100% |
With sodium hydroxide; oxygen; lead acetate; palladium on activated charcoal In water at 150℃; under 7600 Torr; for 1h; | 90.3% |
With potassium phosphate; carbon dioxide; CrH6Mo6O24(3-)*3H3N*3H(1+) In dimethyl sulfoxide at 80℃; under 750.075 Torr; for 24h; Green chemistry; | 90% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 1h; | 100% |
With pyridine 1.) from -20 deg C to 30 deg C, 2.) room temp., 2 h; | 65% |
With pyridine at 0℃; |
Conditions | Yield |
---|---|
With pyridine In benzene for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With ammonium cerium(IV) nitrate; iodine for 8h; Heating; | 100% |
propan-1-ol
4-hydroxyphenylpropionic acid
3-(4-hydroxyphenyl)propionic acid propyl ester
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 25℃; for 24h; | 100% |
With 3 A molecular sieve; sulfuric acid for 72h; Heating; | |
With hydrogenchloride Heating; | |
With chloro-trimethyl-silane at 25℃; for 24h; |
propan-1-ol
3-(2-vinyloxyethoxy)-1,2-propylene carbonate
4-[2-(1-Propoxy-ethoxy)-ethoxymethyl]-[1,3]dioxolan-2-one
Conditions | Yield |
---|---|
With heptafluorobutyric Acid at 20 - 45℃; for 0.333333h; | 100% |
propan-1-ol
(2R,3R,4S,5S)-2,3,4,5-Tetrahydroxy-piperidine-1-carboxylic acid benzyl ester
Conditions | Yield |
---|---|
With hydrogen; acetic acid; palladium on activated charcoal In methanol for 0.5h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With magnesium sulfate In dichloromethane | 100% |
propan-1-ol
(2R,4R)-(-)-6-fluoro-2,3-dihydro-2',5'-dioxospiro<4H-1-benzopyran-4,4'-imidazolidine>-2-carboxylic acid
(2R,4R)-6-fluoro-2,3-dihydro-2',5'-dioxospiro<4H-1-benzopyran-4,4'-imidazolidine>-2-carboxylic acid n-propyl ester
Conditions | Yield |
---|---|
sulfuric acid In benzene for 5h; Heating; | 100% |
propan-1-ol
1,3-Dimethyl-6-chlorouracil
1,3-Dimethyl-6-propoxy-1H-pyrimidine-2,4-dione
Conditions | Yield |
---|---|
With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane; water for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
In pyridine; ethyl acetate | 100% |
propan-1-ol
2-ethyl-1,2-oxaphospholan-5-one 2-oxide
3-(ethylpropoxyphosphinyl)propionic acid
Conditions | Yield |
---|---|
at 20 - 34℃; | 100% |
propan-1-ol
2-ethyl-1,2-oxaphospholan-5-one 2-oxide
Conditions | Yield |
---|---|
at 0 - 15℃; | 100% |
propan-1-ol
N,N'-dibenzyl-2,3,5,6-piperazinetetraone
1,3-Dibenzyl-2-hydroxy-4,5-dioxo-imidazolidine-2-carboxylic acid propyl ester
Conditions | Yield |
---|---|
for 6h; Heating; | 100% |
Conditions | Yield |
---|---|
With chloro-trimethyl-silane for 2h; Heating; | 100% |
Conditions | Yield |
---|---|
Heating; | 100% |
propan-1-ol
ethyl 4,7-dihydro-2-methyl-7-oxopyrazolo[1,5-a]pyrimidine-6-carboxylate
Conditions | Yield |
---|---|
With titanium(IV) isopropylate Heating; | 100% |
propan-1-ol
rimonabant
Conditions | Yield |
---|---|
at 4 - 20℃; Heating / reflux; | 100% |
at 5 - 50℃; for 5h; |
propan-1-ol
bisphenol AF bisoxalyl chloride adduct
Conditions | Yield |
---|---|
In dichloromethane at -35 - 20℃; for 3h; Cooling with isopropanol/dry ice/water; | 100% |
propan-1-ol
Conditions | Yield |
---|---|
In benzene excess of alcohol, stirring, reflux (20h); evapn. under a pressure of 0.3 mm (room temp.), drying at 50-60°C, elem. anal.; | 100% |
Conditions | Yield |
---|---|
In toluene boiling a mixt. of D-mannitol, H3BO3, and n-propanol in toluene on a Dean-Stark apparatus (azeotropic removal of H2O);; removal of toluene and propanol; elem. anal.;; | 100% |
Conditions | Yield |
---|---|
With hydrogenchloride In 1,4-dioxane at 100℃; for 3h; Sealed tube; | 100% |
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen at 50℃; under 37503.8 Torr; | 100% |
propan-1-ol
cis-1,3,5-cyclohexane tricarboxylic acid
cis,cis-tri-n-propyl cyclohexane-1,3,5-tricarboxylate
Conditions | Yield |
---|---|
With hydrogenchloride for 3h; Reflux; | 100% |
propan-1-ol
2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isoselenocyanate
O-n-propyl-N-(2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl)selenocarbamate
Conditions | Yield |
---|---|
at 70℃; for 2h; Inert atmosphere; Darkness; | 100% |
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