The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
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Cas:13175-44-5
Min.Order:1 Kilogram
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inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:13175-44-5
Min.Order:1 Kilogram
FOB Price: $9.0 / 99.0
Type:Trading Company
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Product name: 7-Octen-1-ol CAS No.: 13175-44-5 Molecule Formula:C8H16O Molecule Weight:128.21 Purity: 99.0% Package: 25kg/drum Description:White crystalline powder Manufacture Standards:Enterprise Standard TESTING
Cas:13175-44-5
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryHigh quality,stable supply chain.Appearance:white/off-white or light yellow Storage:Store in cool and dry place, keep away from strong light and heat. Package:aluminum bottle,glass bottle,PTFE bottle,cardboard drum Application:This product can be use
Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:crystalline powder Storage:Room temperature with sealed well Package:according to the clients requirement Application:Use as pri
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 7-Octen-1-ol, CAS:13175-44-5 with the most competitive price and the best quality. We
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Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
oct-7-yn-1-ol
oct-7-en-1-ol
Conditions | Yield |
---|---|
With hydrogen; Lindlar's catalyst In methanol for 0.75h; | 94% |
Conditions | Yield |
---|---|
A 92% B n/a |
tert-butyl dimethyl(oct-7-en-1-yloxy)silane
oct-7-en-1-ol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In methanol at 30℃; for 1h; | 91% |
oct-7-en-1-ol
Conditions | Yield |
---|---|
With rhenium(VII) oxide; triphenylphosphine at 165℃; for 1h; | 90% |
1,7-Octadiene
oct-7-en-1-ol
Conditions | Yield |
---|---|
Stage #1: 1,7-Octadiene With zirconium(IV) chloride; diisobutylaluminium hydride In hexane; toluene at 20℃; for 7h; Stage #2: With oxygen In hexane; toluene at 20 - 40℃; for 4h; Stage #3: With sulfuric acid In hexane; toluene at 0 - 20℃; Further stages.; | 74% |
Stage #1: 1,7-Octadiene With zirconium(IV) chloride; diisobutylaluminium hydride In hexane; toluene at 25℃; for 7h; Inert atmosphere; Stage #2: With sulfuric acid; oxygen In hexane; toluene at 25℃; for 1h; | 60% |
Stage #1: 1,7-Octadiene With borane-THF In tetrahydrofuran at 0℃; for 0.333333h; Inert atmosphere; Stage #2: With dihydrogen peroxide; sodium hydroxide In tetrahydrofuran at -20 - 20℃; Inert atmosphere; | 32% |
Conditions | Yield |
---|---|
Stage #1: vinyl magnesium bromide With copper(l) iodide In tetrahydrofuran; hexane at -40℃; for 0.25h; Inert atmosphere; Stage #2: 1-iodohexan-6-ol With N,N,N,N,N,N-hexamethylphosphoric triamide; triethyl phosphite In tetrahydrofuran; hexane at -40 - 20℃; for 3h; Inert atmosphere; | 71% |
1-(2-tetrahydropyranyloxy)-7-octene
oct-7-en-1-ol
Conditions | Yield |
---|---|
With phosphoric acid |
8-hydroxy-octan-2-one
oct-7-en-1-ol
Conditions | Yield |
---|---|
aluminum oxide Heating; |
oct-7-en-1-yl acetate
oct-7-en-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
Conditions | Yield |
---|---|
With D-glucose 6-phosphate; spinach ferredoxin reductase; Pseudomonas oleovorans monooxygenase; Pseudomonas oleovorans rubredoxin; NADPH In acetone at 25℃; for 0.166667h; Product distribution; Mechanism; withouth NADPH, other products; |
oct-7-enal
oct-7-en-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In methanol for 0.666667h; Ambient temperature; | 14 mg |
Conditions | Yield |
---|---|
In water at 130 - 140℃; Heating; Yield given; |
Conditions | Yield |
---|---|
In water at 130 - 140℃; Product distribution; Heating; |
(8-Hydroxy-octyl)-trimethyl-ammonium; hydroxide
A
8-methoxyoct-1-ene
B
oct-7-en-1-ol
C
dimethylamino-8 octanol-1
D
dimethylamino-1 methoxy-8 octane
Conditions | Yield |
---|---|
at 110 - 120℃; Product distribution; |
5-(tetrahydro-2H-pyran-2-yloxy)pentylmagnesium bromide
allyl bromide
oct-7-en-1-ol
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; copper(l) iodide 1.) THF, 2 deg C, 10 min, 2.) THF, a) 2 deg C, 4 h, b) 20 deg C, 15 h; Yield given. Multistep reaction; |
1,7-Octadiene
A
1,8-Octanediol
B
octanol
C
6-octen-1-ol
D
oct-7-en-1-ol
Conditions | Yield |
---|---|
Stage #1: 1,7-Octadiene With triisobutylaluminum; bis-triphenylphosphine-palladium(II) chloride In dichloromethane at 25℃; for 12h; Stage #2: With sodium hydroxide; oxygen In dichloromethane | A 14 % Spectr. B 21 % Spectr. C 23 % Spectr. D 20 % Spectr. |
oct-7-enoic acid methyl ester
oct-7-en-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether |
azelaic monomethyl ester
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: lead tetraacetate 2: LiAlH4 / diethyl ether View Scheme |
Tetrahydrofurfuryl chloride
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 80 percent / LiNH2 / liquid ammonia / 3 h 2: 90 percent / NaNH2, H2N(CH2)3NH2 / 2.5 h / 80 °C 3: 94 percent / H2 / Pd-CaCO3 / methanol / 0.75 h View Scheme |
4-octyne-1-ol
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 90 percent / NaNH2, H2N(CH2)3NH2 / 2.5 h / 80 °C 2: 94 percent / H2 / Pd-CaCO3 / methanol / 0.75 h View Scheme |
nona-1,8-diene
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 220 mg / N-methylmorpholine-N-oxide / OsO4 / acetone; 2-methyl-propan-2-ol; H2O / 12 h / Ambient temperature 2: 19 mg / NaIO4 / tetrahydrofuran; H2O / 0.5 h / Ambient temperature 3: 14 mg / NaBH4 / methanol / 0.67 h / Ambient temperature View Scheme |
8-nonen-1,2-diol
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 19 mg / NaIO4 / tetrahydrofuran; H2O / 0.5 h / Ambient temperature 2: 14 mg / NaBH4 / methanol / 0.67 h / Ambient temperature View Scheme |
(Z)-Cyclooctene
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 550 °C 2: (i) iBu2AlH, heptane, Et2O, (ii) (oxidation) View Scheme |
1,8-Octanediol
oct-7-en-1-ol
Conditions | Yield |
---|---|
With scandium(III) oxide In ethanol at 350℃; for 5h; Inert atmosphere; | |
Heating; |
2,7-octadiene-1-ol
A
oct-7-en-1-ol
B
oct-7-enal
C
2,7-octadienal
Conditions | Yield |
---|---|
With hydrogen In 1,4-dioxane at 180℃; under 760.051 Torr; for 7h; Temperature; Autoclave; Inert atmosphere; |
1-bromo-6-hexanol
oct-7-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: acetone; sodium iodide / 16 h / Inert atmosphere; Reflux 2.1: copper(l) iodide / hexane; tetrahydrofuran / 0.25 h / -40 °C / Inert atmosphere 2.2: 3 h / -40 - 20 °C / Inert atmosphere View Scheme |
oct-7-en-1-ol
tert-butyldimethylsilyl chloride
tert-butyl dimethyl(oct-7-en-1-yloxy)silane
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In dichloromethane at 0℃; for 3h; | 100% |
With 1H-imidazole In dichloromethane at 20℃; | 55.2% |
oct-7-en-1-ol
2,2'-bipyridine-5-carbonyl chloride
oct-7-enyl-2,2'-bipyridine-5-carboxylate
Conditions | Yield |
---|---|
With triethylamine In chloroform-d1; dichloromethane at -10 - 20℃; for 48h; Inert atmosphere; | 100% |
oct-7-en-1-ol
8-Bromo-1-octene
Conditions | Yield |
---|---|
With carbon tetrabromide; triphenylphosphine In dichloromethane at 0℃; for 1h; | 99% |
With phosphorus tribromide In benzene at 80℃; for 2h; | 80% |
With phosphorus tribromide In dichloromethane at 0 - 20℃; for 2h; | 16.6% |
oct-7-en-1-ol
oct-7-enal
Conditions | Yield |
---|---|
With tetrapropylammonium perruthennate; 4 A molecular sieve; 4-methylmorpholine N-oxide In dichloromethane at 20℃; for 2.5h; | 98% |
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In dimethyl sulfoxide at 20℃; Inert atmosphere; | 97% |
With potassium peroxymonosulfate; sodium ortho-iodobenzenesulfonate; sodium sulfate In nitromethane at 70℃; for 2h; | 92% |
oct-7-en-1-ol
7-hydroxyheptanoic acid
Conditions | Yield |
---|---|
Stage #1: oct-7-en-1-ol With ozone In water; acetonitrile at 0℃; Inert atmosphere; Stage #2: With sodium chlorite In water; acetonitrile at 15 - 20℃; under 760.051 Torr; Inert atmosphere; Stage #3: With sodium hydrogen sulfate In water; acetonitrile at 35℃; for 0.166667h; Inert atmosphere; | 98% |
1-methyl-2(1H)-quinoxalinone
1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
oct-7-en-1-ol
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In 1-methyl-pyrrolidin-2-one at 25℃; for 16h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; | 98% |
Conditions | Yield |
---|---|
With acetic anhydride at 55 - 60℃; for 2h; Inert atmosphere; | 98% |
oct-7-en-1-ol
8-iodo-oct-1-ene
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; iodine; triphenylphosphine In dichloromethane at 0℃; for 1h; | 96% |
With 1H-imidazole; iodine; triphenylphosphine In tetrahydrofuran at 0℃; for 2h; Inert atmosphere; Darkness; | 70% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at -78 - 20℃; for 1.08333h; Inert atmosphere; Schlenk technique; Cooling with acetone-dry ice; | 95% |
With pyridine In dichloromethane at -78℃; Inert atmosphere; |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at -78 - 20℃; for 1.08333h; Inert atmosphere; Schlenk technique; Cooling with acetone-dry ice; | 94% |
Conditions | Yield |
---|---|
With [(η-cyclopentadienyl)(η-benzene)ruthenium] hexafluorophosphate In acetone for 1h; Inert atmosphere; Photolysis; | 93% |
oct-7-en-1-ol
Octanal
Conditions | Yield |
---|---|
With potassium hydroxide; PS-resin; potassium hexacyanoferrate(III); 4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl In water; toluene at 20℃; for 24h; | 92% |
Conditions | Yield |
---|---|
With 1,10-Phenanthroline; palladium(II) trifluoroacetate; triethylamine at 20℃; for 48h; Inert atmosphere; Schlenk technique; | 92% |
oct-7-en-1-ol
A
(E)-5-octene-1-ol
B
(E)-2-octenyl alcohol
Conditions | Yield |
---|---|
With acetonitrile(cyclopentadienyl)[2-(di-i-propylphosphino)-4-(t-butyl)-1-methyl-1H-imidazole]ruthenium(II) hexafluorophosphate In [(2)H6]acetone at 20℃; Inert atmosphere; Schlenk technique; Glovebox; | A n/a B 92% |
Conditions | Yield |
---|---|
Stage #1: oct-7-en-1-ol With sodium hydride In tetrahydrofuran; mineral oil at 0℃; for 0.333333h; Inert atmosphere; Stage #2: C35H54FN3O8Si In tetrahydrofuran; mineral oil at 0 - 23℃; for 2.03333h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane at 0 - 20℃; Inert atmosphere; | 91% |
oct-7-en-1-ol
tetraphenyldiphosphine disulfide
Conditions | Yield |
---|---|
In dichloromethane for 6h; Sealed tube; Inert atmosphere; Irradiation; | 91% |
Conditions | Yield |
---|---|
With pyridine at 25℃; for 48h; | 90% |
With triethylamine In dichloromethane at 20℃; | 29.3% |
oct-7-en-1-ol
7-octenyl chloride
Conditions | Yield |
---|---|
With pyridine; thionyl chloride In toluene at 5 - 15℃; for 10h; Temperature; Reagent/catalyst; | 90% |
With 5-ethyl-2-methyl-pyridine; hydrogenchloride In cyclohexane at 55 - 65℃; for 10h; |
oct-7-en-1-ol
Conditions | Yield |
---|---|
With disodium hydrogenphosphate; Selectfluor; 9-(2-mesityl)-10-methylacridinium perchlorate In water; acetonitrile at 25℃; for 16h; Schlenk technique; Inert atmosphere; Sealed tube; Irradiation; | 90% |
oct-7-en-1-ol
4-iodobenzoic acid ethyl ester
ethyl 4-(8-oxooctyl)benzoate
Conditions | Yield |
---|---|
With lithium acetate; tetrabutyl-ammonium chloride; palladium diacetate; lithium chloride In N,N-dimethyl-formamide at 70℃; for 24h; | 88.3% |
With lithium acetate; tetrabutyl-ammonium chloride; palladium diacetate; lithium chloride In N,N-dimethyl-formamide at 70℃; for 3h; Heck Reaction; | 87% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; dibenzoyl peroxide for 24h; Heating; | 88% |
Conditions | Yield |
---|---|
Stage #1: 4-bromo-phenol; oct-7-en-1-ol With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 18h; Mitsunobu reaction; Inert atmosphere; Stage #2: With sodium hydroxide; water In tetrahydrofuran | 87% |
oct-7-en-1-ol
phenyl 3-O-benzyl-4,6-O-benzyliden-2-(2'-naphthylmethyl)-1-thio-α-D-mannopyranoside
7'-octenyl 2-O-benzyl-4,6-O-benzyliden-β-D-mannopyranoside
Conditions | Yield |
---|---|
Stage #1: phenyl 3-O-benzyl-4,6-O-benzyliden-2-(2'-naphthylmethyl)-1-thio-α-D-mannopyranoside With 1-hexene; 1-benzenesulfinyl piperidine; 2,4,6-tri-tert-butylpyrimidine In dichloromethane at -78℃; for 0.25h; Molecular sieve; Stage #2: With trifluoromethylsulfonic anhydride In dichloromethane at -78℃; for 0.166667h; Molecular sieve; Stage #3: oct-7-en-1-ol In dichloromethane at -78 - 20℃; for 2.5h; Molecular sieve; | 86% |
Conditions | Yield |
---|---|
at 100℃; | 85% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In neat (no solvent) at 80℃; for 5h; Solvent; Green chemistry; | 85% |
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