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:112-31-2
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inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
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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
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inquiryShanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
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inquiryOur 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
LIDE PHARMACEUTICALS LIMITED is a professional chemicals and APIs leading manufacturer in China. Our core business line covers APIs, Intermediates, Herb extract, etc.
With our good experience, we offer detailed technical support and advice to assist customers. We communicate closely with customers to establish their quality requirements. Consistent Quality Our plant has strict quality control in each manufacturin
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inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
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inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developmen
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inquiryAppearance:colourless liquid Storage:R T Package:25kg/Barrel Application:Used in organic synthesis and as a fragrance. It is often used as a blending raw material for flavors such as iris, orange blossom, frangipani, fragrant leaves, pansy, rose, et
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inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
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Cas:112-31-2
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inquiryProduct Name: Decyl aldehyde CAS: 112-31-2 MF: C10H20O MW: 156.27 EINECS: 203-957-4 Decyl aldehyde Structure Decyl aldehyde Chemical Properties Melting point 7 °C Boiling point 207-209 °C (lit.) density 0.83 g/mL
Packing: According to customer requirements Delivery time: In stock or depands Port of shipment: Ningbo/Shanghai/Qingdao OEM/ODM:Welcome Sample:We can offer our existing samples at once Appearance:Colorless liquid / Refer to COA Storage:Store b
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inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
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Cas:112-31-2
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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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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 o
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
GMP standard, high purity, competitive price, in stock 1. Quick Response: within 6 hours after receiving your email. 2. Quality Guarantee: All products are strictly tested by our QC, confirmed by QA, and approved by a third-party lab in China, USA,
Hangzhou 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
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Name Decanal Synonyms Caprinaldehyde; Decyl aldehyde CAS NO. 112-31-2 Molecular Formula C10H20O Molecular Weight 156.26 EINECS 203-957-4 FEMA
High 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
Luyunjia Chemistry Xiamen Limited is a high-tech company specializing in R&D and manufacturing of photoinitiators monomers and oligomers, UV absorbers and pharmaceutical intermediates, and pharmaceutical intermediates of generic drug. and has a h
Cas:112-31-2
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inquiryfactory Storage:Shading, sealed and preserved. Package:Grams, Kilograms Application:An organic synthetic intermediate used Transportation:According to customer request Port:Qingdao
Conditions | Yield |
---|---|
With air; poly-alkylated (nitrosyl)Ru(salen) In benzene-d6 at 20℃; for 12h; Irradiation; | 100% |
With air; 1-Phenylethanol; (nitrosyl)Ru(salen) In benzene-d6 at 20℃; for 24h; Product distribution; Further Variations:; Catalysts; Temperatures; Irradiation; | 100% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxygen; copper(I) bromide dimethylsulfide complex In chlorobenzene at 90℃; for 7h; | 100% |
2-nonyl-1,3-dithiane
caprinaldehyde
Conditions | Yield |
---|---|
With tetrafluoroboric acid; mercury(II) oxide In tetrahydrofuran Ambient temperature; | 100% |
With K-10 clay supported iron(III) nitrate nonahydrate In dichloromethane for 4h; Ambient temperature; with K-10 clay-supported copper(II) nitrate trihydrate; | 99.1% |
With nitric acid; arsenic(III) trioxide In dichloromethane at 0 - 5℃; | 96% |
With iodine; silver nitrate In tetrahydrofuran for 6h; Ambient temperature; | 88% |
Conditions | Yield |
---|---|
With water In tetrahydrofuran; diethyl ether at 80℃; under 6000.6 Torr; Inert atmosphere; Autoclave; | 100% |
With C11H10N2O2Pd(1+)*ClO4(1-); water In acetonitrile at 50℃; Reagent/catalyst; Temperature; | 96% |
With polymer-supported dicyanoketene acetal; water In acetonitrile at 20℃; for 0.5h; Hydrolysis; | 17% |
Multi-step reaction with 2 steps 1: 92 percent / CH2Cl2 / 0.5 h / 0 °C 2: 100 percent / PPTS; water / acetone / 2 h View Scheme |
decanal diethyl acetal
caprinaldehyde
Conditions | Yield |
---|---|
With water In tetrahydrofuran; diethyl ether at 80℃; under 6000.6 Torr; Inert atmosphere; Autoclave; | 100% |
indium(III) chloride In methanol; water for 1.41667h; Heating; | 96% |
Stage #1: decanal diethyl acetal With 2,4,6-trimethyl-pyridine; triethylsilyl trifluoromethyl sulfonate In dichloromethane at 0℃; for 2h; Stage #2: With water In dichloromethane for 0.1h; | 85% |
caprinaldehyde
Conditions | Yield |
---|---|
With water; pyridinium p-toluenesulfonate In acetone for 2h; | 100% |
Conditions | Yield |
---|---|
With C71H80N3P2Ru*F6P(1-); water In acetone at 60℃; for 18h; Inert atmosphere; | 99% |
With benzo[1,3,2]dioxaborole In tetrahydrofuran for 12h; Heating; hydroboration of alkenes and alkynes; var. reaction partners; | 90% |
With cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate; 5,5′-bis(trifluoromethyl)-2,2′-bipyridine In 1-methyl-pyrrolidin-2-one; water at 25℃; for 24h; Inert atmosphere; Autoclave; | 90% |
Conditions | Yield |
---|---|
With silica gel; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium perchlorate In dichloromethane | A 99% B n/a |
With oxygen at 60℃; under 760.051 Torr; for 24h; Irradiation; | A 6% B 47% |
With 4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl; sodium hydrogencarbonate; pyridinium hydrobromide perbromide In dichloromethane; water at 0 - 4℃; | |
With 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; iodine; sodium hydrogencarbonate In dichloromethane; water at 20 - 22℃; for 3h; | A 22 %Chromat. B 16 %Chromat. |
In hexane at 180℃; for 5h; | A 7 %Chromat. B 12 %Chromat. |
caprinaldehyde
Conditions | Yield |
---|---|
With 9-borabicyclo[3.3.1]nonane dimer In tetrahydrofuran for 1h; Ambient temperature; | 98% |
Conditions | Yield |
---|---|
With thexylchloroborane-Me2SO4 In dichloromethane for 0.25h; Ambient temperature; | 97% |
With thexylbromoborane dimethyl sulfide complex In carbon disulfide; dichloromethane at -20 - 20℃; for 1h; | 94% |
With 9-borabicyclo[3.3.1]nonane dimer; lithium dihydrido borata-bicyclo[3.3.0]nonane In tetrahydrofuran for 1h; Ambient temperature; | 92% |
Conditions | Yield |
---|---|
With tetra-N-butylammonium tribromide In methanol at 20℃; for 0.25h; | 97% |
With sodium hydrogen sulfate; PEG-2000 at 70℃; for 0.583333h; | 88% |
With iron(II) sulfate In toluene for 10h; Heating; Yield given; |
Conditions | Yield |
---|---|
With trimethylamine-N-oxide In dimethyl sulfoxide for 24h; Ambient temperature; | 95% |
A
caprinaldehyde
Conditions | Yield |
---|---|
With titanium tetrachloride In dichloromethane at -78℃; Yields of byproduct given; | A n/a B 95% |
Conditions | Yield |
---|---|
With iron(III) chloride In dichloromethane for 1h; Product distribution; Ambient temperature; other solvent, temperature; | 95% |
indium(III) chloride In methanol; water for 1.41667h; Heating; | 86% |
With 2,6-dimethylpyridine; trimethylsilyl trifluoromethanesulfonate In dichloromethane at 0℃; for 0.5h; | 79% |
n-decanal oxime
caprinaldehyde
Conditions | Yield |
---|---|
With γ-picolinium chlorochromate In dichloromethane at 20℃; for 4h; | 95% |
With potassium permanganate; montmorillonite K-10 for 0.833333h; | 93% |
With γ-picolinium chlorochromate; silica gel In dichloromethane at 20℃; for 8h; | 91% |
4-(4-Methoxy-phenyl)-2-nonyl-[1,3]dioxolane
caprinaldehyde
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane; water Ambient temperature; | 94% |
2-Nonyl-benzo[1,3]oxathiole
caprinaldehyde
Conditions | Yield |
---|---|
With tetrafluoroboric acid; mercury(II) oxide In tetrahydrofuran Ambient temperature; | 92% |
With tetrafluoroboric acid; mercury(II) oxide In tetrahydrofuran Product distribution; Ambient temperature; various 1,3-benzoxathioles; | 92% |
2-nonyl-1,3-oxathiolane
caprinaldehyde
Conditions | Yield |
---|---|
With perchloric acid; dihydrogen peroxide; ammonium bromide; molybdic acid In dichloromethane at 0 - 5℃; for 1.5h; | 90% |
With Glyoxilic acid; Amberlyst 15 at 80℃; for 3h; | 80% |
Conditions | Yield |
---|---|
With potassium carbonate | 90% |
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; trimethylsilyl trifluoromethanesulfonate In benzene at 80℃; for 10h; | 89% |
methanol
1-decenyl dimethyl phosphate
A
trimethyl phosphite
B
caprinaldehyde
Conditions | Yield |
---|---|
With cesium fluoride at 65℃; for 22h; | A 67% B 88% |
1-decenyl dimethyl phosphate
A
trimethyl phosphite
B
caprinaldehyde
Conditions | Yield |
---|---|
With methanol; cesium fluoride at 65℃; for 22h; | A 67% B 88% |
Conditions | Yield |
---|---|
With 9-borabicyclo[3.3.1]nonane dimer In tetrahydrofuran for 1h; Ambient temperature; | 88% |
1,1-Bis-ethylsulfanyl-decane
caprinaldehyde
Conditions | Yield |
---|---|
With K-10 clay supported copper(II) nitrate trihydrate In dichloromethane for 3h; Ambient temperature; with K-10 clay-supported iron(III) nitrate nonahydrate; | 87.5% |
With K-10 clay supported copper(II) nitrate trihydrate In dichloromethane for 3h; Ambient temperature; K-10 clay supported iron(III) nitrate nonahydrate; | 87.5% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); α,α,α-trifluorotoluene; tri-n-butyl-tin hydride at 80℃; under 60800 Torr; for 2h; | A 87% B 8% |
Conditions | Yield |
---|---|
With zirconocene dichloride; lithium tri-t-butoxyaluminum hydride In tetrahydrofuran at 20℃; for 0.0333333h; Inert atmosphere; | 87% |
Multi-step reaction with 2 steps 1: Ti(O-i-Pr)4, Ph2SiH2 / 20 °C 2: 1 M aq. HCl / tetrahydrofuran / 20 °C View Scheme |
Conditions | Yield |
---|---|
With dimethyl sulfoxide for 0.0666667h; Kornblum oxidation; Microwave irradiation; | 85% |
With trimethylamine-N-oxide In dimethyl sulfoxide for 5h; Ambient temperature; | 81% |
With 4-methylmorpholine N-oxide; 1-ethyl-3-methyl-1H-imidazol-3-ium chloride; potassium iodide at 100℃; for 0.0833333h; Microwave irradiation; Ionic liquid; | 80% |
A
caprinaldehyde
Conditions | Yield |
---|---|
With diisobutylaluminium hydride In tetrahydrofuran at -10 - 20℃; for 0.5h; | A 83% B n/a |
caprinaldehyde
Conditions | Yield |
---|---|
With hydrogenchloride In tetrahydrofuran; water at 30℃; for 4h; | 83% |
3,4,4-Trimethyl-2-nonyl-oxazolidine
caprinaldehyde
Conditions | Yield |
---|---|
With oxonium | 82% |
1-(dimethylphenylsilyl)decan-1-ol
caprinaldehyde
Conditions | Yield |
---|---|
With chromium(VI) oxide In dimethyl sulfoxide at 25℃; | 82% |
Conditions | Yield |
---|---|
With selenium(IV) oxide; dihydrogen peroxide In tetrahydrofuran for 4h; Heating; | 100% |
With palladium 10% on activated carbon; water; sodium hydroxide at 80℃; under 600.06 Torr; for 6h; | 99% |
With dihydrogen peroxide In acetic acid at 90℃; for 7h; | 97% |
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate; magnesium sulfate In dichloromethane for 2h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; Bu3SnCl-BF3; tert.-butyl lithium In tetrahydrofuran -78 deg C to r.t.; | 100% |
caprinaldehyde
Conditions | Yield |
---|---|
With pyridine In dichloromethane at 20℃; for 5h; Addition; | 100% |
caprinaldehyde
decanoyl azide
Conditions | Yield |
---|---|
With sodium azide; Iodine monochloride In acetonitrile at 25℃; for 2.5h; | 100% |
caprinaldehyde
n-decanal hydrazone
Conditions | Yield |
---|---|
With hydrazine hydrate at 100℃; | 100% |
caprinaldehyde
(S)-2-amino-3-phenylpropionamide hydrochloride
(5S)-5-benzyl-2-nonylimidazolidin-4-one
Conditions | Yield |
---|---|
With potassium carbonate; triethylamine In ethanol at 60℃; for 24h; | 100% |
caprinaldehyde
tert-butyl 1-(2-methylallyl)hydrazinecarboxylate
tert-butyl 2-decylidene-1-(2-methylallyl)hydrazinecarboxylate
Conditions | Yield |
---|---|
In ethanol at 20℃; for 24h; Inert atmosphere; | 100% |
caprinaldehyde
ethyl 2-cyanoacetate
ethyl 2-amino-5-octylthiophene-3-carboxylate
Conditions | Yield |
---|---|
With sulfur; triethylamine In ethanol at 60℃; Inert atmosphere; | 100% |
With sulfur; triethylamine In ethanol Inert atmosphere; |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 120℃; for 15h; Inert atmosphere; Schlenk technique; | 100% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 120℃; for 15h; Inert atmosphere; Schlenk technique; | 100% |
Conditions | Yield |
---|---|
With sodium butanolate In butan-1-ol Reflux; | 100% |
Conditions | Yield |
---|---|
With C43H42N2O4P2Ru; hydrogen In isopropyl alcohol at 100℃; under 22801.5 Torr; for 24h; Pressure; Glovebox; Autoclave; | 99% |
antimony(III) chloride; aluminium In water; N,N-dimethyl-formamide for 3h; Ambient temperature; | 98% |
With water; antimony(III) chloride; aluminium In N,N-dimethyl-formamide for 3h; Ambient temperature; | 98% |
caprinaldehyde
1,4-dibromo-2-(bromomethyl)but-2-ene
Conditions | Yield |
---|---|
With zinc In N,N-dimethyl-formamide at 0℃; for 2h; | 99% |
With zinc In tetrahydrofuran 1.) reflux, 2 h; 2.) room. temp., 2 h; | 87% |
Conditions | Yield |
---|---|
In diethyl ether at -42 - 20℃; for 2h; | 99% |
In tetrahydrofuran for 4h; | 33% |
With water 1) Et2O, 0 deg C to r.t., 2 h; Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In acetic acid for 1h; Ambient temperature; | 99% |
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h; | 95% |
With tetrabutylammomium bromide at 90 - 100℃; for 3.7h; | 91% |
caprinaldehyde
Methyl diethylphosphonoacetate
methyl (E)-dodec-2-enolate
Conditions | Yield |
---|---|
With sodium hydride In tetrahydrofuran at -78 - 25℃; Condensation; Wadsworth-Emmons reaction; | 99% |
caprinaldehyde
Ethyl bromodifluoroacetate
2,2-difluoro-3-hydroxydodecanoic acid ethyl ester
Conditions | Yield |
---|---|
With zinc In tetrahydrofuran at 20℃; for 3h; | 99% |
With zinc In tetrahydrofuran Condensation; Heating; | 56% |
With chloro-trimethyl-silane; ethylene dibromide; zinc In tetrahydrofuran | 53% |
With zinc In tetrahydrofuran Condensation; Reformatsky reaction; | 46% |
Conditions | Yield |
---|---|
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h; | 99% |
polyaniline sulphate salt In dichloromethane at 20℃; for 6h; | 65% |
With perchloric acid In dichloromethane at 0 - 5℃; for 2h; | 57% |
Conditions | Yield |
---|---|
Stage #1: n-butyl magnesium bromide With zirconocene dichloride In tetrahydrofuran; toluene at 0℃; for 0.5h; Stage #2: With 2,4-dimethylpentan-3-one In tetrahydrofuran; toluene at 0℃; for 3h; Stage #3: caprinaldehyde In tetrahydrofuran; toluene at 25℃; for 5h; | 99% |
caprinaldehyde
3-trimethylsilyl-2-diethylphosphonopropionic acid ethyl ester
(E)-2-Trimethylsilanylmethyl-dodec-2-enoic acid ethyl ester
Conditions | Yield |
---|---|
With sodium hydride In 1,2-dimethoxyethane at 0℃; Wittig-Horner reaction; | 99% |
Conditions | Yield |
---|---|
With hydroquinone; p-benzoquinone In water at 20℃; for 3h; Reagent/catalyst; Solvent; Knoevenagel Condensation; Inert atmosphere; Sealed tube; | 99% |
With Na8H[PW9O34]*7H2O In methanol at 25℃; for 6h; Knoevenagel Condensation; | 82% |
With morpholine In ethanol at 20℃; for 0.0833333h; Knoevenagel condensation; | |
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; | 88 %Chromat. |
With 1-dodecyl-3-(3-triethoxysilylpropyl)-4,5-dihydroimidazolium bromide grafted onto layered double hydroxide In water at 20℃; for 5h; Knoevenagel Condensation; | 87 %Chromat. |
Conditions | Yield |
---|---|
With 4-methyl-N-[(1R)-2-{[(1S,2S)-2-{[(2R)-2-(4-methylbenzenesulfonamido)-2-phenylethyl]amino}-1,2-diphenylethy]amino}-1-phenylethyl]benzene-1-sulfonamido; copper(II) acetate monohydrate In ethanol at 20℃; for 48h; Henry reaction; Inert atmosphere; optical yield given as %ee; enantioselective reaction; | 99% |
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