As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:110-43-0
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inquiryOur advantage: 1: High quality and Competitive price 2: Quality control, GC&HPLC&NMR or as your requested 3: Packing as your requested, and double check before shipment 4: Prompt shipment with professional documents 5: Excellent after-
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inquiryThe 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
Our company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
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inquiryProduct Name 2-Heptanone CAS No. 110-43-0 Appearance Colorless liquid Assay ≥9
Product Detail Minimum Order Qty. 10 Gram
Cas:110-43-0
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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
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:110-43-0
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inquiryMETHYL AMYL KETONEAppearance:colorless liquid Storage:Store tightly sealed under inert gas in a cool, well-ventilated area. Package:according to customers' requirements Application:Flavor & Fragrance Transportation:By air(EMS or EUB or FedEx or TNT e
Superior quality, moderate price & quick delivery. Appearance:pale yellow to yellow liquid Storage:Store in a cool, dry and ventilated place Package:200L/drum or as you required Application:Widely used in the fields in the industrial solvent, f
We are leading fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...)
Cas:110-43-0
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inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
SAGECHEM is a chemical R&D, manufacturing and distribution company in China since 2009, including pharmaceutical intermediates, agrochemical, dyestuff intermediates, organosilicone, API and etc. We also offer a full range of services in
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inquiryISO Factory/Good qualityAppearance:off white Storage:dry and cool place Package:10G/BAG; 1KG/BAG ;25KG/DRUM Application:Active pharaceutical ingredients Transportation:BY SEA,AIR,EXPRESS Port:SHANGHAI;BEIJING
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R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:110-43-0
Min.Order:1 Kilogram
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Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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Xiamen Luyunjia Trading Co.,Ltd Package:1kg/bag; 728kg/drum, or as customer's request. Application:Xiamen Luyunjia Trading Co.,Ltd Transportation:DHL, EMS, FedEx, TNT, AIR, SEA Port:Beijing,Shanghai,Guangzhou ,China main port
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
low price and high purityAppearance:solid or liquid Storage:in sealed air resistant place Package:As customer require Application:Pharma;Industry;Agricultural Transportation:by sea or by airplane Port:any port in China
2-Heptanol
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With tert.-butylhydroperoxide; [O-Cu4(triethanolamine)4(BOH)4][BF4]2 In acetonitrile at 69.84℃; for 7h; | 100% |
With dihydrogen peroxide; bromine In dichloromethane; water at 20℃; for 2h; | 99% |
With pyridine In dichloromethane at 20℃; for 5h; | 96% |
C7H14OS
n-pentyl methyl ketone
Conditions | Yield |
---|---|
Ambient temperature; | 100% |
Ambient temperature; Yield given; |
2-Methyl-2-pentyl-1,3-dithiolane
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With t-butyl bromide; dimethyl sulfoxide at 70 - 75℃; for 4h; | 100% |
With trimethylsilyl bromide; dimethyl sulfoxide In tetrachloromethane at 75 - 80℃; for 24h; | 95% |
With thionyl chloride; dihydrogen peroxide In acetonitrile at 25℃; for 0.0333333h; | 92% |
Conditions | Yield |
---|---|
With Pd(II)(15-crown-5-phen)Cl2; dinitrogen monoxide In N,N-dimethyl acetamide; water at 150℃; under 2250.23 Torr; for 18h; | 99% |
With 2(p-CH2-C6H4CN)2[(CH2)3SO3Na]2-calix[4]arene*PdCl2; oxygen; copper dichloride under 3750.3 Torr; for 2h; Wacker oxidation; | 89% |
With dihydrogen peroxide In water; acetonitrile at 55℃; for 12h; Wacker Oxidation; | 77% |
Conditions | Yield |
---|---|
With silica gel; iron(III) chloride at 20℃; for 0.0833333h; | 98% |
With pyridinium chlorochromate at 45℃; for 2.5h; | 91% |
With thiourea In ethanol; water for 6h; Heating; | 89% |
With γ-picolinium chlorochromate In dichloromethane at 20℃; for 12h; | 75% |
Conditions | Yield |
---|---|
With zinc dichromate trihydrate at 20℃; grinding; neat (no solvent); chemoselective reaction; | 97% |
With 3-carboxypyridinium dichromate In acetonitrile at 20℃; for 0h; | 96% |
With potassium permanganate; iron(II) sulfate In dichloromethane for 5h; Heating; | 86% |
With potassium permanganate; copper(II) sulfate In dichloromethane for 24h; Heating; | 68 % Chromat. |
Conditions | Yield |
---|---|
With disodium chloro[1,3-bis(2,6-diisopropyl-4-sodiumsulfonatophenyl)imidazol-2-ylidene]gold(I); water at 100℃; for 1.17h; | 96% |
With C22H20AuN3O2P(1+)*CF3O3S(1-); water; silver trifluoromethanesulfonate; acetic acid at 100℃; for 10h; | 92% |
With water; trans-Bu4N[Au(2,4,6-C6F5)2Cl2] In methanol for 1.5h; Product distribution; Further Variations:; Catalysts; Heating; | 90% |
Conditions | Yield |
---|---|
With [(COD)Ir(dimethylphenylphosphine)(1,3-bis(2,4,6-trimethylphenyl)imidazolin-2-ylidene)](tetrakis(3,5-bis(trifluoromethyl)phenyl)borate); hydrogen In dichloromethane at -78 - 25℃; under 760.051 Torr; for 2h; chemoselective reaction; | 95% |
With 1% Pd/C; hydrogen |
2,2'-dimethoxyheptane
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With water; Nafion-H In acetone for 0.5h; | 94% |
With Bi(1+)*NO3(1-)=BiNO3 In dichloromethane at 20℃; for 2h; | 78% |
Conditions | Yield |
---|---|
With vanadium(III) chloride In tetrahydrofuran for 8h; Ambient temperature; | 92% |
With phosphotungstic acid; bismuth (III) nitrate pentahydrate at 40 - 45℃; for 0.333333h; | 86% |
With tert.-butylhydroperoxide In tetrachloromethane for 18h; Heating; | 80% |
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With trimethylsilyl trifluoromethanesulfonate; nitrobenzaldehyde polymer In dichloromethane for 3h; Ambient temperature; | 89% |
With 4-nitrobenzaldehdye; trimethylsilyl trifluoromethanesulfonate In dichloromethane for 0.0833333h; Ambient temperature; | 88% |
3-aminoheptan-2-one
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With potassium bisulfite; 2-nitro-phenyl hypochlorite at 65℃; for 9h; Temperature; | 89% |
Conditions | Yield |
---|---|
With 1,4-dichloro-1,4-diazoniabicyclo[2,2,2]octane bischloride In water at 50℃; for 0.25h; pH=7; | 87% |
With dihydrogen peroxide; vanadyl acetylacetonate In acetone at 20℃; for 8h; | 82% |
Conditions | Yield |
---|---|
With potassium hydroxide; 18-crown-6 ether In ethanol; benzene 1.) room temperature, 16 h, 2.) reflux, 2 h; | 86% |
at 525℃; | |
Darstellung; |
Conditions | Yield |
---|---|
With methanol; sodium chloride electrolysis; | 85% |
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With cerium(III) chloride; silica gel for 0.0666667h; Microwave irradiation; | 85% |
lithium salt of 2-heptanol
A
1,1-Diphenylmethanol
B
n-pentyl methyl ketone
C
2-Heptanol
Conditions | Yield |
---|---|
With benzophenone In tetrahydrofuran at 24℃; for 96h; | A 78% B 15% C 84% |
lithium salt of 2-heptanol
A
n-pentyl methyl ketone
B
2-Heptanol
Conditions | Yield |
---|---|
With benzophenone In tetrahydrofuran at 24℃; Mechanism; | A 15% B 84% |
trans-3-hepten-2-ol
4-chlorophenyl acetate
A
n-pentyl methyl ketone
B
trans 3-hepten-2-one
Conditions | Yield |
---|---|
With RuCl3H(p-cymene)2; immobilized lipase from Pseudomonas cepacia; triethylamine In dichloromethane at 20 - 25℃; for 48h; Acetylation; oxidation; reduction; Enzymatic reaction; | A n/a B n/a C 83% |
Conditions | Yield |
---|---|
Heating; | A 83% B n/a |
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With bis(acetylacetonato)dioxidomolybdenum(VI); dihydrogen peroxide In acetone at 20℃; for 10h; | 82% |
1-Trimethylsilanyl-heptan-2-one
A
n-pentyl methyl ketone
B
1-chloro-2-heptanone
Conditions | Yield |
---|---|
With sulfuryl dichloride; triethylamine In dichloromethane 1.) 0 deg C, 2.) room temperature; Yields of byproduct given; | A n/a B 76% |
1,1-dibromohept-1-ene
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With water; zinc at 275℃; for 4h; | 76% |
C9H18B(1-)*Li(1+)
A
2-Methyl-2-heptanol
B
n-pentyl methyl ketone
C
hex-1-yne
Conditions | Yield |
---|---|
With sodium hydroxide; methanesulfonic acid; dihydrogen peroxide 1.) Et2O, -78 deg C, warming to 25 deg C, 2h; Yield given. Multistep reaction; | A 8% B n/a C 73% |
With sodium hydroxide; methanesulfonic acid; dihydrogen peroxide 1.) Et2O, -78 deg C warming to 25 deg C, 2h; Yield given. Multistep reaction; | A 8% B 9% C n/a |
Conditions | Yield |
---|---|
With formic acid; dodecacarbonyl-triangulo-triruthenium for 2.5h; Heating; | A 14% B 72% |
3-hepten-2-one
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With aluminum tri-bromide; cyclohexane In various solvent(s) at 20℃; for 40h; | 70% |
With ethanol; nickel pumice stone under 4560 Torr; Hydrogenation; | |
With NADPH-dependent curcumin/dihydrocurcumin reductase from Escherichia coli DH10B; NADPH Enzymatic reaction; |
Conditions | Yield |
---|---|
With CZYE medium (Biolife) In water for 24h; Colletotrichum gloeosporoides CBS 193.32; | A 70% B n/a |
2-heptyl-hypochlorite
A
2-ethyl-5-methyl-tetrahydro-furan
B
n-pentyl methyl ketone
C
2-Heptanol
D
5-Chloro-heptan-2-ol
Conditions | Yield |
---|---|
With sodium hydrogencarbonate; iron(II) sulfate In tetrachloromethane Ambient temperature; protected from the light; | A 7% B 5% C n/a D 68% |
C14H21NO2
n-pentyl methyl ketone
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 70℃; | 68% |
Conditions | Yield |
---|---|
With water; palladium dichloride at 25℃; under 1300 Torr; for 22h; in microemulsion system, closed reactor; | 66% |
n-pentyl methyl ketone
2-Heptanol
Conditions | Yield |
---|---|
With sodium aluminum tetrahydride In tetrahydrofuran at 0℃; for 0.0833333h; | 100% |
Stage #1: n-pentyl methyl ketone With sodium tetrahydroborate at 25℃; for 0.5h; Ball milling; neat (no solvent); Stage #2: With water regiospecific reaction; | 100% |
Stage #1: n-pentyl methyl ketone With C35H55Cl2NRuS; isopropyl alcohol at 82℃; for 0.166667h; Stage #2: With potassium hydroxide at 82℃; for 1h; Reagent/catalyst; | 100% |
n-pentyl methyl ketone
4-chlorobenzaldehyde
(E)-1-(4-chlorophenyl)oct-1-en-3-one
Conditions | Yield |
---|---|
Stage #1: n-pentyl methyl ketone With piperidine In ethanol at 20℃; for 2h; Stage #2: 4-chlorobenzaldehyde In ethanol for 72h; Reflux; | 100% |
barium dihydroxide In ethanol for 1h; Heating; | 93% |
n-pentyl methyl ketone
2-Amino-2-methyl-1-propanol
2,4,4-trimethyl-2-pentyloxazolidine
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene Heating; | 100% |
Conditions | Yield |
---|---|
With (R)-3,3'-bis(2,4,6-triisopropylphenyl)binol phosphoric acid; 2-(3,5-dimethylphenyl)indoline In 1,3,5-trimethyl-benzene at 20 - 80℃; for 72h; Molecular sieve; Inert atmosphere; enantioselective reaction; | 100% |
With 2-Phenylbenzothiazolin; C51H59O4P In benzene at 20℃; for 48h; Molecular sieve; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 77% |
Conditions | Yield |
---|---|
With 2.5% wt Pd/C; hydrogen at 160℃; for 3h; Catalytic behavior; Dean-Stark; chemoselective reaction; | 100% |
n-pentyl methyl ketone
trimethylsilyl cyanide
2-methyl-2-(trimethylsiloxy)heptanenitrile
Conditions | Yield |
---|---|
With potassium carbonate at 20℃; for 6h; | 99% |
With N,N-dimethyl-(2-hydroxybenzyl)amine N-oxide In diethyl ether at 23℃; for 0.5h; | 99% |
With 1-methoxy-2-methyl-1-(trimethylsiloxy)propene at 25℃; for 50h; | 99% |
n-pentyl methyl ketone
ethane-1,2-dithiol
2-Methyl-2-pentyl-1,3-dithiolane
Conditions | Yield |
---|---|
With silica gel; zirconium(IV) chloride In dichloromethane Ambient temperature; < 5 min; | 99% |
With cobalt(II) bromide In dichloromethane for 0.5h; Ambient temperature; | 98% |
With P-benzyltriphenylphosphonium tribromide at 20℃; for 1.5h; | 96% |
With P-benzyltriphenylphosphonium tribromide In dichloromethane at 20℃; for 7h; | 90% |
With phosphorus pentoxide; silica gel for 0.0666667h; | 86% |
Conditions | Yield |
---|---|
With Montmorillonite KSF In benzene for 12h; Heating; | 99% |
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; 1,2-bis(dimethylphosphanyl)ethane; bis(pinacol)diborane In toluene at 50℃; for 18h; | 99% |
With trifluoroacetic acid; cobalt(II) bromide; zinc In acetonitrile at 20℃; for 5h; | 65% |
With manganese; trifluoroacetic acid; zinc dibromide; FeBr2(bpy) In N,N-dimethyl-formamide at 80℃; for 5h; | 61% |
With [2,2]bipyridinyl; tetrabutylammonium tetrafluoroborate; iron(II) bromide In N,N-dimethyl-formamide at 20℃; Electrochemical reaction; | 60% |
n-pentyl methyl ketone
naphthalene-2-sulfonate
4-amino-o-xylene
N-2-heptyl-3,4-xylidine
Conditions | Yield |
---|---|
With hydrogen; platinum | 99% |
n-pentyl methyl ketone
(3,4-dimethoxyphenyl)methanol
1-(3,4-dimethoxyphenyl)octan-3-one
Conditions | Yield |
---|---|
With potassium phosphate; 5%-palladium/activated carbon In 5,5-dimethyl-1,3-cyclohexadiene at 130℃; for 24h; Temperature; Inert atmosphere; | 99% |
With potassium phosphate In toluene at 110℃; for 24h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
titanium tetrachloride In chloroform at -10 - 30℃; for 6h; | 98% |
With sodium sulfate; zinc(II) chloride |
Conditions | Yield |
---|---|
In diethyl ether at -30 - 0℃; for 2h; | 98% |
n-pentyl methyl ketone
hydrogen cyanide
carbon dioxide
5-methyl-5-n-amylhydantoin
Conditions | Yield |
---|---|
Stage #1: n-pentyl methyl ketone With gallium(III) triflate; ammonia In dichloromethane at -78℃; for 3h; Inert atmosphere; Stage #2: hydrogen cyanide In dichloromethane at -78 - 25℃; Inert atmosphere; Stage #3: carbon dioxide With N-ethyl-N,N-diisopropylamine In dichloromethane at 25℃; for 7h; Inert atmosphere; | 98% |
Conditions | Yield |
---|---|
In toluene at 20℃; | 98% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate at 20℃; Neat (no solvent); | 97% |
With sodium tetrahydroborate; silica phosphoric acid In tetrahydrofuran at 20℃; for 0.2h; | 94% |
With sodium tetrahydroborate; silica-gel-supported sulfuric acid at 20℃; for 0.0333333h; Neat (no solvent); regioselective reaction; | 93% |
With borohydride exchange resin; triethylamine hydrochloride In ethanol for 1h; Ambient temperature; | 89% |
n-pentyl methyl ketone
benzene-1,2-diol
2-methyl-2-n-pentyl-1,3-benzodioxole
Conditions | Yield |
---|---|
With Montmorillonite KSF In toluene for 12h; Heating; | 97% |
With toluene-4-sulfonic acid In toluene for 10h; Heating; | 90% |
Conditions | Yield |
---|---|
With lithium hydroxide at 140℃; for 48h; Inert atmosphere; | 97% |
With potassium phosphate; aluminum oxyhydroxide; palladium In toluene at 110℃; for 3h; | 90% |
With potassium phosphate tribasic trihydrate; C39H32Cl2N5PRu In tert-Amyl alcohol at 120℃; for 12h; Inert atmosphere; Schlenk technique; | 79% |
Conditions | Yield |
---|---|
With Na8H[PW9O34]*7H2O In methanol at 25℃; for 6h; Knoevenagel Condensation; | 96% |
With molybdenum hexacarbonyl at 140℃; for 5h; Inert atmosphere; | 95% |
With ammonium acetate; acetic acid | |
With 0.04O40PW12(3-)*0.73Mg(2+)*0.22Al(3+)*2HO(1-)*0.98H2O In water; isopropyl alcohol at 60℃; for 6h; Knoevenagel Condensation; chemoselective reaction; | 97 %Chromat. |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; third-generation glucose-persubstituted amidoamine dendrimer In tetrahydrofuran at -80℃; | 96% |
With sodium tetrahydroborate; D-gluconamide PAMAM dendrimer G(3)G In tetrahydrofuran at -80℃; | 96% |
With dried cells of Geotrichum candidum; NAD; isopropyl alcohol In various solvent(s) at 30℃; for 20h; pH=7.0; Enzymatic reaction; | 89% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate at 20℃; for 0.25h; | 96% |
With sodium tetrahydroborate at 20℃; for 0.0333333h; Neat (no solvent); grinding; | 96% |
With sodium tetrahydroborate In tetrahydrofuran at 20℃; for 0.0833333h; | 95% |
Conditions | Yield |
---|---|
With hydrogen; K-10 montmorillonite; platinum In diethylene glycol dimethyl ether under 37503 Torr; for 24h; Reduction; | 96% |
n-pentyl methyl ketone
4-methoxy-aniline
N-(heptan-2-yl)-4-methoxyaniline
Conditions | Yield |
---|---|
With formic acid; C39H48ClIrN2O; sodium formate In water at 50℃; for 12h; pH=4.8; | 96% |
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