DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:928-96-1
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inquiryProduct Description
Cas:928-96-1
Min.Order:1 Kilogram
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inquiryIterms Standard Appearance Colorless oily liquid Odor Strong green grass odor Relative Density (
cis-3-Hexen-1-ol Product name:cis-3-Hexen-1-ol Molecular formula:C6H12O Structural formula:CH3CH2CH=CHCH2CH2OH Molecular weight:l00.16 CAS No.:928-96-1 Appearance:colorless oily liquid or light yellow liquid Density:0.8508g/cm3。 Boilin
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
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Cas:928-96-1
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Cas:928-96-1
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Cas:928-96-1
Min.Order:1 Gram
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Cas:928-96-1
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Cas:928-96-1
Min.Order:1 Kilogram
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Min.Order:10 Gram
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Cas:928-96-1
Min.Order:10 Gram
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inquiryProduct Name: Leaf alcohol CAS: 928-96-1 MF: C6H12O MW: 100.16 EINECS: 213-192-8 Mol File: 928-96-1.mol Leaf alcohol Structure Leaf alcohol Chemical Properties Melting point 22.55°C (estimate) Boiling point 156-157 &de
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
Cas:928-96-1
Min.Order:1 Kilogram
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Type:Trading Company
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Min.Order:1 Kilogram
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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Min.Order:10 Milligram
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inquiryMinimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
Cas:928-96-1
Min.Order:10 Gram
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Type:Trading Company
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Cas:928-96-1
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryAppearance:white powder/crystal Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:Used for research and industrial manufacture. Transportation:Common products:Sea/A
Cas:928-96-1
Min.Order:100 Metric Ton
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Type:Lab/Research institutions
inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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Why Choose Us: 1. Factory direct sales, so we can provide the competitive price and high quality product base on 8 years of production and R&D experience. 2. It is available in stock for quick shipment.Products could be packaged according to cu
Conditions | Yield |
---|---|
With hydrogen; N,N′-bis(salicylidene)-ethylenediamino‑palladium In pyridine for 0.283333h; | 100% |
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760.051 Torr; | 99% |
With trichlorosilane; silica gel; acetic acid; tetrakis(triphenylphosphine) palladium(0) In dichloromethane for 3h; Ambient temperature; | 96% |
Conditions | Yield |
---|---|
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A 99% B n/a |
With hydrogen In methanol at 30℃; under 760.051 Torr; for 3h; | A 99% B 1% |
With hydrogen In methanol at 20℃; under 150.015 - 900.09 Torr; for 0.0116667h; Inert atmosphere; Schlenk technique; Green chemistry; | A n/a B n/a |
2,4-hexadiene-1-ol
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
C
hex-4-en-1-ol
D
hexan-1-ol
Conditions | Yield |
---|---|
With hydrogen; (methyl benzoate)Cr(CO)6 In methanol at 190 - 200℃; under 36775.4 Torr; for 2h; | A 92.5% B 4.6% C 2.3% D 0.6% |
With hydrogen; (1,2,4,5-tetramethylbenzene)tricarbonylchromium(0) In methanol at 190 - 200℃; under 36775.4 Torr; for 4h; Product distribution; other arene ligands, other solvents; also in absence of arene ligands; |
3-hexyn-1-ol
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
C
hexan-1-ol
Conditions | Yield |
---|---|
With hydrogen In methanol at 20℃; under 1800.18 Torr; Catalytic behavior; Reagent/catalyst; | A 88% B n/a C n/a |
With hydrogen; poly(N-vinyl-2-pyrrolidone)-stabilised Pd-nanoclusters In methanol at 29℃; | |
With hydrogen In isopropyl alcohol at 30℃; under 2250.23 Torr; for 20h; Autoclave; optical yield given as %de; stereoselective reaction; |
Sorbyl alcohol
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
With Na12(Ga4(1,5-bis(2,3-dihydroxybenzamido)naphthalene))6; [(DMPE)Rh(COD)][BF4]; hydrogen In water-d2 at 20℃; for 12h; | 84% |
With hydrogen; chromium(0) hexacarbonyl In hexane at 160 - 180℃; under 38000 - 60800 Torr; for 4h; | |
With hydrogen; [(η5-C5Me5)Ru(η4-MeCH=CHCH=CHCO2H)] triflate In ethylene glycol at 40℃; under 15001.5 Torr; for 0.42h; Catalytic hydrogenation; |
Conditions | Yield |
---|---|
With 1% Rh/Al2O3; hydrogen; iron In ethanol at 120℃; under 15001.5 Torr; for 4h; Reagent/catalyst; Temperature; Pressure; Solvent; Autoclave; | 80.35% |
With aldehyde reductase; nicotinamide adenine dinucleotide phosphate Enzymatic reaction; |
6-methyl-3,6-dihydro-2H-pyran
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
With calcium; ethylenediamine at 90℃; for 8h; | 60% |
homoalylic alcohol
diethylaluminium chloride
A
3-methyl-1-pentanol
B
(Z)-3-Hexen-1-ol
C
(E)-3-hexen-1-ol
D
butan-1-ol
E
hexan-1-ol
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane at -45℃; for 2h; Mechanism; Product distribution; variation of added base; | A 13% B 3% C 18% D 20% E 21% |
Conditions | Yield |
---|---|
With Pd-BaSO4; benzene at 50℃; Hydrogenation; | |
With lithium; Trimethylenediamine at 25℃; for 2h; | |
With palladium/highly-ordered mesoporous silica supported 3-D pore network(3.7) 1-phenylethan-1-amine 0.02 for 2.91667h; | |
With hydrogen In methanol at 20℃; under 862.586 Torr; for 8h; Catalytic behavior; Flow reactor; | A n/a B n/a |
cis/trans-3-chloro-2-ethyltetrahydrofuran
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
Conditions | Yield |
---|---|
With samarium diiodide In tetrahydrofuran Product distribution; Heating; using dipolar-aprotic cosolvents; | |
With samarium diiodide In tetrahydrofuran for 5h; Heating; Yield given. Yields of byproduct given; |
6-methyl-3,6-dihydro-2H-pyran
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
C
(E)-hex-4-en-1-ol
Conditions | Yield |
---|---|
With lithium In various solvent(s) at -78℃; Yield given. Yields of byproduct given; |
Conditions | Yield |
---|---|
With lithium In various solvent(s) Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
dimethylaluminum chloride In n-heptane; dichloromethane at 25℃; Yield given. Yields of byproduct given; |
3-hexyn-1-ol
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
C
4-hexyn-1-ol
D
hexan-1-ol
Conditions | Yield |
---|---|
With lithium; Trimethylenediamine at 60℃; for 1.33333h; Product distribution; other compounds containing a triple bond and/or an aromatic ring; var. temp., time; |
(3R,4R)-3,4-Dibromo-hexan-1-ol
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
With tetrabutylammonium tetrafluoroborate In N,N-dimethyl-formamide -1.4 V (vs. SCE) at a mercury pool (divided cell); Yield given; |
2-Chlorobutanal
ethyl acetate
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
Conditions | Yield |
---|---|
Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
3-chloro-2-vinyltetrahydrofuran
A
5-Hexen-1-ol
B
(Z)-3-Hexen-1-ol
C
(E)-3-hexen-1-ol
D
(E)-hex-4-en-1-ol
Conditions | Yield |
---|---|
With sodium In diethyl ether Yield given. Yields of byproduct given; | |
With sodium In toluene Yield given. Yields of byproduct given; |
2-hydroxymethyl-5-methyl-2,5-dihydrothiophene
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
Conditions | Yield |
---|---|
With lithium In various solvent(s) Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With hydrogen; chromium(0) hexacarbonyl In methanol at 190 - 200℃; under 36775.4 Torr; for 4h; Yield given. Yields of byproduct given; | |
With hydrogen; [Ru(C5(1,2,4-tBu3)H2)(1,3-COD)]BF4 In acetone at 70℃; under 3750.38 Torr; Product distribution / selectivity; | |
With diphenyl-phosphinic acid; hydrogen; [Ru(C5(1,2,4-tBu3)H2)(1,3-COD)]BF4 In acetone at 70℃; under 3750.38 Torr; Product distribution / selectivity; |
methyl (Z)-hex-3-enoate
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate; zinc 2-ethylhexanoate 1.) THF, 70 deg C, 4 h, 2.) 40 deg, 1 h; Yield given; Multistep reaction; |
Conditions | Yield |
---|---|
at -18℃; Hydrogenation; |
tetrachloromethane
3-hexyn-1-ol
A
(Z)-3-Hexen-1-ol
B
(E)-3-hexen-1-ol
Conditions | Yield |
---|---|
at 100℃; Hydrogenation; |
Conditions | Yield |
---|---|
at 50℃; Hydrogenation; |
Conditions | Yield |
---|---|
at 21 - 23℃; under 843 Torr; Hydrogenation; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaBH4 / H2O / 2 h / Ambient temperature 2: H2 / Cr(CO)6 / methanol / 4 h / 190 - 200 °C / 36775.4 Torr View Scheme | |
Multi-step reaction with 2 steps 1: NaBH4 / H2O / 2 h / Ambient temperature 2: 92.5 percent / H2 / (methyl benzoate)Cr(CO)6 / methanol / 2 h / 190 - 200 °C / 36775.4 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: LiAlH4 / diethyl ether 3: Li / various solvent(s) View Scheme |
methyl 5-methylthiophene-2-carboxylate
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: LiAlH4 / diethyl ether 2: Li / various solvent(s) View Scheme |
5-methyl-2,5-dihydrothiophene-2-carboxylic acid
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 2: LiAlH4 / diethyl ether 3: Li / various solvent(s) View Scheme |
Methyl 2,5-Dihydro-5-methyl-2-thiophenecarboxylate
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: LiAlH4 / diethyl ether 2: Li / various solvent(s) View Scheme |
(Z)-3-Hexen-1-ol
N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide
1,1-dimethylethyl (Z)-3-hexenyl[(4-methylphenyl)sulfonyl]carbamate
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0℃; | 100% |
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran for 3h; Ambient temperature; | 88% |
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 20℃; for 6h; Mitsunobu reaction; | 74% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane | 100% |
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 0℃; |
Conditions | Yield |
---|---|
Stage #1: (Z)-3-Hexen-1-ol; triphenylphosphine With 1H-imidazole In dichloromethane at 0℃; for 0.333333h; Stage #2: With iodine In dichloromethane at 0 - 20℃; for 3h; Stage #3: triphenylphosphine In acetonitrile for 19h; Reflux; | 100% |
(Z)-3-Hexen-1-ol
2-(3-ethyloxiran-2-yl)ethan-1-ol
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; C14H17BrMoN2O2 In dichloromethane at 54.84℃; for 24h; Reagent/catalyst; | 99% |
With Oxone; ethylenediaminetetraacetic acid; tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; acetone In water; acetonitrile for 4h; | 90% |
With dihydrogen peroxide; sodium acetate; ortho-tungstic acid In methanol; water at 20℃; for 16h; pH=4.5; | 49% |
Conditions | Yield |
---|---|
zinc(II) perchlorate In diethyl ether for 7h; Heating; | 99% |
Conditions | Yield |
---|---|
zinc(II) perchlorate at 20℃; for 1.83333h; | 99% |
(Z)-3-Hexen-1-ol
triisopropylsilyl chloride
Conditions | Yield |
---|---|
With 1H-imidazole In dichloromethane at 20℃; for 1h; Inert atmosphere; | 99% |
(Z)-3-Hexen-1-ol
1-benzyloxyallene
Conditions | Yield |
---|---|
With trans-1,2-(1S,2S)-1,2-diaminocyclohexane-N,N’-bis(2’-diphenylphosphinobenzoyl); tris-(dibenzylideneacetone)dipalladium(0); triethylamine In dichloromethane at 20℃; for 20h; Inert atmosphere; | 99% |
(Z)-3-Hexen-1-ol
methanesulfonyl chloride
methanesulfonic acid hex-3(Z)-enyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; for 1.5h; | 98% |
With triethylamine In dichloromethane for 0.5h; Ambient temperature; | 97% |
With pyridine at 0 - 20℃; for 6h; | 91% |
Conditions | Yield |
---|---|
With zinc diacetate at 50℃; for 9h; | 98% |
Conditions | Yield |
---|---|
With cobalt(II) chloride at 60℃; for 10h; | 97% |
(Z)-3-Hexen-1-ol
Conditions | Yield |
---|---|
With tributylphosphine; di-isopropyl azodicarboxylate In tetrahydrofuran; toluene at 20℃; for 1h; Mitsunobu Displacement; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With indium(III) chloride In chloroform at 20℃; for 5h; | 96% |
Conditions | Yield |
---|---|
With cerium(III) chloride; sodium iodide at 25℃; for 6h; | 96% |
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 0 - 20℃; for 4h; | 95% |
With pyridine In dichloromethane at 0 - 20℃; for 4h; | 95% |
With pyridine In dichloromethane at 0 - 20℃; | 95% |
Conditions | Yield |
---|---|
With dmap; diisopropyl-carbodiimide In dichloromethane at 0 - 20℃; | 94% |
(Z)-3-Hexen-1-ol
(3R,4R)-3,4-Dibromo-hexan-1-ol
Conditions | Yield |
---|---|
With pyridinium perbromide hydrobromide In chloroform at -60 - -10℃; | 93% |
(Z)-3-Hexen-1-ol
2-((2SR,3RS)-3-ethyloxiran-2-yl)ethan-1-ol
Conditions | Yield |
---|---|
With sodium hydroxide; dihydrogen peroxide; N-tosylimidazole In methanol for 3h; | 93% |
With dihydrogen peroxide; ethenetetracarbonitrile In acetonitrile for 12h; Product distribution; Ambient temperature; other olefins, var. reagents (tetracyanoethylene oxide, carbonyl cyanide), var. temp.; | 92% |
With dihydrogen peroxide; ethenetetracarbonitrile In acetonitrile for 12h; Ambient temperature; | 92% |
(Z)-3-Hexen-1-ol
Benzoylformic acid
(Z)-3-hexenyl 2-oxo-2-phenylacetate
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 48h; | 93% |
for 2h; Heating; Yield given; |
(Z)-3-Hexen-1-ol
(Z)-hex-3-en-1-yl sulfamate
Conditions | Yield |
---|---|
With formic acid; isocyanate de chlorosulfonyle In N,N-dimethyl acetamide at 20℃; | 93% |
With formic acid; isocyanate de chlorosulfonyle In N,N-dimethyl acetamide at 0 - 20℃; | 93% |
With sulphamoyl chloride; triethylamine In acetonitrile at 0 - 23℃; Inert atmosphere; | 69% |
(Z)-3-Hexen-1-ol
(3Z)-1-chloro-3-hexene
Conditions | Yield |
---|---|
With thionyl chloride; N,N-dimethyl-formamide In dimethyl sulfoxide at 5 - 25℃; for 3h; Concentration; | 92% |
With pyridine; thionyl chloride; chloroform | |
With pyridine; thionyl chloride In chloroform | |
With pyridine; thionyl chloride In hexane | |
Multi-step reaction with 2 steps 1: pyridine / CH2Cl2 / 16 h / 20 °C 2: 1.5 g / LiCl / acetone View Scheme |
Conditions | Yield |
---|---|
With pyridine; dmap In dichloromethane for 24h; | 92% |
With pyridine; benzene |
(Z)-3-Hexen-1-ol
tert-butylchlorodiphenylsilane
(Z)-tert-butyl(hex-3-en-1-yloxy)diphenylsilane
Conditions | Yield |
---|---|
With 1H-imidazole; triethylamine In dichloromethane at 20℃; for 16h; Inert atmosphere; | 92% |
With 1H-imidazole; diisopropylamine In dichloromethane for 40h; Ambient temperature; |
Conditions | Yield |
---|---|
With iodine In dichloromethane at 23℃; for 0.583333h; Prins-cyclization; | 92% |
(Z)-3-Hexen-1-ol
3,5-Bis(1,1-dimethylethyl)-4-methoxy-benzoic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; Inert atmosphere; | 92% |
(Z)-3-Hexen-1-ol
(Z)-3-hexenyl iodide
Conditions | Yield |
---|---|
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 1h; | 91% |
(i) TsCl, Py, (ii) NaI, acetone; Multistep reaction; | |
Multi-step reaction with 2 steps 1: 60 percent / pyridine / 8 h / 20 °C 2: NaI / acetonitrile / 3 h / 70 °C View Scheme |
(Z)-3-Hexen-1-ol
methyl 2-oxocyclopentane-1-carboxylate
Conditions | Yield |
---|---|
With N,N-3-diethylaminopropylated silica gel In xylene for 3.5h; Heating; | 91% |
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