Dayangchem’s 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. DayangChem can provide different quantiti
Cas:108-91-8
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inquiryWe are manufacturer of this product. If you are looking for the material's manufacturer or supplier in China, Ality Group is your best choice. Specifications of our Cyclohexylamine CAS 108-91-8: Items Spe
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Cas:108-91-8
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inquiryProduct description: Product name Cyclohexylamine CAS number 108-91-8 Assay ≥99.5% Appearance Colorless transparent liquid Capacity 5000mt/year Application Rubber auxiliaries
Cas:108-91-8
Min.Order:1 Kilogram
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inquiryISO 9001 certificate Good quality Competive price On time delivery Appearance:colorless clear liquid Storage:Ventilated warehouse temperature drying; And oxidant, acid Package:170kg/drum Application:Cas 108-91-8 Used for rubber vulcanization
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inquiryOur 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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inquiryChemical Name: Cyclohexylamine CAS No.: 109-88-6 Molecular Fomula:C6H13N Chemical Structure: Molecular weight: 99.17 Appearance: Colorless Liquid Assay:99.0%min Appearance: Colorless Transparent Liquid Storage: Preserve in well-closed, li
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 present
Cas:108-91-8
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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:108-91-8
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inquiryCyclohexanamine CAS:108-91-8 Specification Product Name Cyclohexylamine CAS No. 108-91-8 EINECS No. 203-629-0 Molecular Formula C6H13N Molecular Weight 99.17 g·mol−
Hangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting CHA (Cyclohexylamine;Aminocyclohexane; Hexahydroaniline) CAS: 108-91-8, Please contact us by email freely. We are leading exporter in China
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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/Ai
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inquiryJ&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
Cas:108-91-8
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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
Cas:108-91-8
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inquiryOur Services 1. New Molecules R&D 2. Own test center HPLC NMR GC LC-MS 3. API and Intermediates from China reputed manufacturers 4. Documents support COA MOA MSDS DMF open part Our advantages 1. Government awarded company. Top 100 enter
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:108-91-8
Min.Order:10 Gram
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inquiryFactory high purity high quanlity 99% low price CyclohexylamineAppearance:Colorless to pale yellow clear liquid Storage:Store in dry,dark,ventilated place Package:according to customers' requirements Application:It is mainly used for Pharmaceutical i
Cas:108-91-8
Min.Order:1 Gram
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inquirysupplier in China Appearance:clear liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum;200kg/drum as per your request Application:Used for rubber vulcanization accelerator, is also used as a raw m
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,
Cas:108-91-8
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inquiryProduct name: Cyclohexylamine CAS No.:108-91-8 Molecule Formula:C6H13N Molecule Weight:99.17 Purity: 99.0% Package: 200kg/drum Description:Colorless to pale yellow liquid Manufacture Standards:Enterprise Standard T
Cas:108-91-8
Min.Order:1 Kilogram
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inquiryWe are leading fine chemicals supplier in China with ISO certificate, Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED
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Min.Order:1 Gram
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Type:Lab/Research institutions
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
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Conditions | Yield |
---|---|
With hydrogen In water at 100℃; under 15001.5 Torr; for 1.5h; | 100% |
Stage #1: aniline With ammonia; hydrogen at 120℃; under 45004.5 Torr; Stage #2: at 150℃; | 97.3% |
With hydrogen; [(norbornadiene)rhodium(I)chloride]2; phosphinated polydiacetylene In n-heptane at 30℃; under 60800 Torr; for 17h; | 80% |
Conditions | Yield |
---|---|
With potassium hydroxide; hydrogen In methanol; water Devarda copper electrode; | 100% |
With carbon monoxide; Au/TiO2-VS; water In ethanol at 25℃; under 3800.26 Torr; for 4h; Autoclave; chemoselective reaction; | 100% |
With indium; ammonium chloride In ethanol Heating; | 100% |
N-(2-hydroxybenzylidene)cyclohexylamine
N-butylamine
A
(E)-2-((butylimino)methyl)phenol
B
cyclohexylamine
Conditions | Yield |
---|---|
In [D3]acetonitrile at 25℃; Equilibrium constant; Molecular sieve; | A 100% B n/a |
Conditions | Yield |
---|---|
In [D3]acetonitrile at 25℃; Equilibrium constant; Molecular sieve; | A 100% B n/a |
Conditions | Yield |
---|---|
In [D3]acetonitrile at 25℃; Equilibrium constant; Molecular sieve; | A 100% B n/a |
Conditions | Yield |
---|---|
With sodium hydroxide at 450℃; for 8h; Temperature; Autoclave; Large scale; | 99.49% |
prop-2'-en-1'-yl cyclohexylcarbamate
cyclohexylamine
Conditions | Yield |
---|---|
With tris(2,2'-bipyridine)nickel(II) tetrafluoroborate In N,N-dimethyl-formamide at 20℃; allyl carbamate cleavage; Electrochemical reaction; Zn/stainless steel couple electrodes; current intensity 60 mA; supporting electrolite: tetrabutylammonium tetrafluoroborate; | 99% |
With aniline; (ϖ-allyl)palladium triflate based catalyst at 30℃; | 99% |
With formic acid; triphenylphosphine; tris(dibenzylideneacetone)dipalladium(0) chloroform complex In tetrahydrofuran at 30℃; for 3h; | 100 % Chromat. |
With trifluorormethanesulfonic acid; [RuCp(η3-C3H5)(QA)]PF6, QA=quinaldic acid In methanol at 30℃; for 2h; | 99 % Spectr. |
Conditions | Yield |
---|---|
With hydrogen In ethanol at 109.84℃; under 18751.9 Torr; for 7.5h; Autoclave; Green chemistry; chemoselective reaction; | 99% |
aniline
A
cyclohexane
B
cyclohexylamine
C
N-cyclohexyl-cyclohexanamine
D
cyclohexene
Conditions | Yield |
---|---|
With ammonia; hydrogen at 180 - 200℃; | A n/a B 98.4% C 0.08% D n/a |
With hydrogen at 160 - 200℃; under 150015 Torr; | A n/a B 95.9% C 0.45% D n/a |
4-Phenyl-2-butanone
cyclohexanone
A
(R)-1-methyl-3-phenylpropylamine
B
cyclohexylamine
Conditions | Yield |
---|---|
With Candida boidinii formate dehydrogenase; pyridoxal 5'-phosphate; Aspergillus terreus ω-trans aminase; Lysinibacillus fusiformis leucine dehydrogenase; ammonium formate; nicotinamide adenine dinucleotide In aq. buffer at 30℃; for 24h; pH=8.8; Catalytic behavior; Green chemistry; Enzymatic reaction; | A 4.5% B 98.2% |
cyclohexyl azide
cyclohexylamine
Conditions | Yield |
---|---|
With magnesium In methanol for 0.25h; | 98% |
With n-butyllithium; dimethylamine borane In tetrahydrofuran 1.) 0 deg C, 30 min; 2.) 25 deg C, 1 h; | 98% |
With sodium sulfide; water for 0.5h; Reflux; | 95% |
(tert-Butyl-diphenyl-silanyl)-cyclohexyl-amine
cyclohexylamine
Conditions | Yield |
---|---|
With pyridine hydrogenfluoride In tetrahydrofuran; water at 25℃; for 2h; Product distribution; | 98% |
With methanol; bromine for 24h; Heating; | 95% |
Conditions | Yield |
---|---|
With lithium hydroxide; hydrogen; 5% ruthenium/lithium aluminate In water at 150℃; under 44718.8 Torr; for 2.08333h; Product distribution / selectivity; Neat (no solvent); | A 97.1% B 1% |
With lithium hydroxide; hydrogen; 5% activated charcoal-supported ruthenium catalyst In water at 150℃; under 44718.8 Torr; for 1.21667h; Product distribution / selectivity; Neat (no solvent); | A 91.8% B 5.73% |
With hydrogen; 5% ruthenium/lithium aluminate at 150℃; under 44718.8 Torr; for 1.28333 - 3h; Product distribution / selectivity; Neat (no solvent); | A 89.2% B 0.08% |
Conditions | Yield |
---|---|
With ammonia; hydrogen In methanol at 30℃; for 6h; Autoclave; | 97% |
With ammonium hydroxide; nickel-aluminum alloy; water at 25℃; for 2h; Temperature; Time; Sonication; Green chemistry; | 91% |
With ammonia; hydrogen In methanol at 90℃; under 15001.5 Torr; for 4h; | 90% |
Conditions | Yield |
---|---|
With potassium tert-butylate; copper diacetate In m-xylene for 8h; Reagent/catalyst; Solvent; Schlenk technique; Heating; chemoselective reaction; | A 96% B n/a C n/a |
Conditions | Yield |
---|---|
With triethylamine alane In tetrahydrofuran for 0.5h; Ambient temperature; | 94% |
With sodium tetrahydroborate; nickel; sodium hydroxide In methanol; water at 20 - 30℃; | 92% |
With sodium hydrogensulfate monohydrate; molybdenum(V) chloride; sodium cyanoborohydride In N,N-dimethyl-formamide for 1.3h; Reflux; | 90% |
Conditions | Yield |
---|---|
With hydrogen In water at 80℃; under 15001.5 Torr; for 4h; Catalytic behavior; Autoclave; | A 6.4% B 93.6% |
With hydrogen; Ph(III) complex In ethanol at 80℃; for 4h; Product distribution; other catalysts; | |
With 5 wt% ruthenium/carbon; hydrogen; sodium nitrite In N,N-dimethyl-formamide at 170℃; under 62256.2 Torr; for 4h; Temperature; Pressure; Solvent; Concentration; Autoclave; |
Conditions | Yield |
---|---|
With ammonium hydroxide; hydrogen; magnesium oxide; ruthenium In water at 99.9℃; under 15001.2 Torr; Product distribution; | A 6.5% B 93.5% |
With ammonia; hydrogen In methanol; ethanol at 100℃; under 37503.8 Torr; for 3h; Catalytic behavior; Reagent/catalyst; Autoclave; | A 93.4% B 6.6% |
With ammonia; hydrogen In methanol at 80℃; for 6h; Autoclave; | A 91% B 9% |
N-phenyl(methylidene)cyclohexanamine
1-phenyl-3,4-dimethylphosphole
B
cyclohexylamine
Conditions | Yield |
---|---|
With iron(II) chloride In toluene at 170℃; for 16h; Inert atmosphere; | A 93% B n/a |
Conditions | Yield |
---|---|
With water; [{Ru(η3:η3-[-CH2C(CH3)=CHCH2]2)(μ-Cl)Cl}2] at 90℃; for 3h; | 92% |
With tert.-butylhydroperoxide; chromia-pillared montmorillonite catalyst (Cr-PILC) In 2,2,4-trimethylpentane; dichloromethane for 20h; Ambient temperature; | 90% |
With polymethylhydrosiloxane; zinc(II) chloride; tetrakis(triphenylphosphine) palladium(0) In tetrahydrofuran at 20℃; | 89% |
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane; water at 20℃; for 24h; chemoselective reaction; | 20% |
Conditions | Yield |
---|---|
thiophenol | 92% |
Conditions | Yield |
---|---|
Stage #1: N-cyclohexylacetamide With Schwartz's reagent In tetrahydrofuran at 20℃; for 0.0333333h; Inert atmosphere; Stage #2: With water In tetrahydrofuran Inert atmosphere; | 91% |
N-(4-methoxybenzylidene)cyclohexylamine
1-phenyl-3,4-dimethylphosphole
B
cyclohexylamine
Conditions | Yield |
---|---|
With iron(II) chloride In toluene at 170℃; for 16h; Inert atmosphere; | A 91% B n/a |
Conditions | Yield |
---|---|
With hydrogen; palladium dihydroxide; palladium on activated charcoal In tetrahydrofuran; water; isopropyl alcohol for 6h; | 90% |
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; laccase from Trametes versicolor; oxygen In aq. buffer at 30℃; for 16h; pH=5; Enzymatic reaction; |
Conditions | Yield |
---|---|
With hydrazine hydrate In 1,4-dioxane at 110℃; Gabriel Amine Synthesis; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; borane-THF In tetrahydrofuran at 25℃; for 144h; | 89% |
With sodium tetrahydroborate; nickel boride In methanol | 66% |
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; borane-THF 1.) 25 deg C, 6 days, 2.) 60 -65 deg C, 2 h, 3.) NaOH; Yield given. Multistep reaction; | |
With hydrogenchloride; sodium tetrahydroborate; boron trifluoride diethyl etherate 1.) THF, reflux, 5.5 h, 2.) heating, 2 h; Yield given. Multistep reaction; |
cyclohexyl-thiophen-2-ylmethylene-amine
1-phenyl-3,4-dimethylphosphole
B
cyclohexylamine
Conditions | Yield |
---|---|
With iron(II) chloride In toluene at 170℃; for 16h; Inert atmosphere; | A 88% B n/a |
Conditions | Yield |
---|---|
With methanol; 5% Rh/C; ammonia; hydrogen; isopropyl alcohol In Hexadecane at 110℃; under 12001.2 Torr; for 16h; Autoclave; | A 88% B n/a |
N-cyclohexyl-1-phenyl-2,2,2-trifluoroethylideneamine
cyclohexylamine
Conditions | Yield |
---|---|
With boric acid In ethanol Heating; | 87% |
succinic acid anhydride
cyclohexylamine
4-(cyclohexylamine)-4-oxobutanoic acid
Conditions | Yield |
---|---|
Stage #1: succinic acid anhydride; cyclohexylamine In N,N-dimethyl acetamide at 20℃; for 24h; Stage #2: In N,N-dimethyl acetamide; xylene at 140℃; for 48h; | 100% |
In 1,4-dioxane at 80℃; for 0.5h; | 90% |
In dichloromethane at 20℃; for 0.333333h; | 89% |
Conditions | Yield |
---|---|
at 100℃; for 12h; Ionic liquid; Green chemistry; | 100% |
In water at 20℃; for 1h; Green chemistry; | 95% |
In water at 20℃; for 0.833333h; Green chemistry; | 95% |
Conditions | Yield |
---|---|
at 90℃; for 1h; microwave irradiation; | 100% |
With immobilization of Candida cylindracea lipase In hexane at 55℃; for 15h; | 99% |
With 1-(3-sulfopropyl)pyridinium phosphotungstate In neat (no solvent) at 100℃; for 0.5h; Microwave irradiation; | 91% |
Conditions | Yield |
---|---|
With sodium hydroxide In water at 25℃; for 1h; | 100% |
Stage #1: cyclohexylamine; benzoyl chloride With pyridine In dichloromethane at 20℃; for 0.333333h; Stage #2: With poly{trans-bicyclo[2.2.1]hept-5-ene-2,3-di(chlorocarbonyl)} In dichloromethane at 20℃; for 0.5h; | 99% |
With pyridine In dichloromethane at 0 - 20℃; | 97% |
Conditions | Yield |
---|---|
In dichloromethane | 100% |
With triethylamine In dichloromethane at 20 - 27℃; for 1h; | 100% |
In acetonitrile at 5 - 20℃; for 2h; | 93% |
Conditions | Yield |
---|---|
In dichloromethane at 0 - 20℃; for 2h; | 100% |
In dichloromethane at 5℃; Inert atmosphere; | 99% |
In dichloromethane at 5 - 20℃; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
In toluene at 25℃; Rate constant; also in DMSO; | 100% |
In toluene at 25℃; | 100% |
97% |
cyclohexylamine
p-toluenesulfonyl chloride
N-cyclohexyl-p-toluenesulfonamide
Conditions | Yield |
---|---|
In dichloromethane at 20℃; for 0.5h; Inert atmosphere; | 100% |
With pyridine at 0 - 25℃; Inert atmosphere; Schlenk technique; | 99% |
With triethylamine In tetrahydrofuran at 0 - 20℃; | 95% |
cyclohexylamine
N,N'-dicyclohexyldiazene N,N'-dioxide
Conditions | Yield |
---|---|
With sodium percarbonate; N,N,N',N'-tetraacetylethylenediamine; sodium hydrogencarbonate In dichloromethane; water for 3h; Ambient temperature; | 100% |
With sodium perborate; N,N,N',N'-tetraacetylethylenediamine; sodium hydrogencarbonate In water; ethyl acetate for 2.5h; Ambient temperature; | 75% |
With peracetic acid |
cyclohexylamine
phosphonic acid diethyl ester
diethyl cyclohexylphosphoramidate
Conditions | Yield |
---|---|
With potassium carbonate; potassium hydrogencarbonate; tetrabutylammomium bromide In tetrachloromethane; dichloromethane at 15 - 20℃; for 2h; | 100% |
With copper(ll) bromide In ethyl acetate at 25℃; for 3h; | 89% |
With tetrachloromethane at 20℃; for 1h; Atherton-Todd Synthesis; | 85% |
Conditions | Yield |
---|---|
With picoline In dichloromethane at 20℃; for 1h; | 100% |
With pyridine In dichloromethane at 0 - 20℃; | 85% |
With pyridine |
4-hydroxyphthalic anhydride
cyclohexylamine
2-cyclohexyl-5-hydroxyisoindoline-1,3-dione
Conditions | Yield |
---|---|
In toluene at 110℃; for 12h; Molecular sieve; Inert atmosphere; | 100% |
In toluene Heating; | 82% |
2,4,6-Tris(4-methylphenoxy)-1,3,5-triazine
cyclohexylamine
(4,6-Bis-p-tolyloxy-[1,3,5]triazin-2-yl)-cyclohexyl-amine
Conditions | Yield |
---|---|
100% |
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) at 100℃; | 100% |
With Cu1-Mo1/TiO2 In neat liquid at 20℃; for 21h; Catalytic behavior; Inert atmosphere; UV-irradiation; | 94% |
With [Cp*Ir(2-(1H-benzo[d]imidazol-2-yl)-1H-benzo[d]imidazole)Cl][Cl]; caesium carbonate at 120℃; for 12h; Schlenk technique; | 94% |
Conditions | Yield |
---|---|
100% | |
In diethyl ether; tetrahydrofyran at 0℃; for 1h; | 96% |
With triethylamine In diethyl ether at 0℃; | 88% |
bromoacetic acid tert-butyl ester
cyclohexylamine
N-cyclohexylglycine t-butyl ester
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In ethanol at 20℃; for 12h; | 100% |
With triethylamine In ethanol Ambient temperature; | |
With sodium hydrogencarbonate In ethanol | 31.9 g (97%) |
o-formylbenzonitrile
cyclohexylamine
3-(cyclohexylamino)isoindolin-1-one
Conditions | Yield |
---|---|
at 20℃; for 9h; | 100% |
With N,N,N,N-tetraethylammonium tetrafluoroborate In acetonitrile at 20℃; Electrolysis; | 60% |
cyclohexylamine
N-bis-(methylsulfanylmethylene)benzenesulfonamide
N1-phenylsulfonyl-N2,N3-dicyclohexylguanidine
Conditions | Yield |
---|---|
for 7h; Heating; | 100% |
(E)-(4-Oxo-2-butenyl)phosphonsaeure-diethylester
cyclohexylamine
(5-aza-5-cyclohexylpenta-2,4-dienyl)diethoxyphosphin-1-one
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; | 100% |
With molecular sieve In tetrahydrofuran Ambient temperature; Yield given; |
(1-Cyan-2-dimethylaminovinyl)phosphonsaeure-diethylester
cyclohexylamine
((Z)-1-Cyano-2-cyclohexylamino-vinyl)-phosphonic acid diethyl ester
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
2-Diethoxyphosphoryl-3-dimethylaminoacrylsaeure-ethylester
cyclohexylamine
(Z)-3-Cyclohexylamino-2-(diethoxy-phosphoryl)-acrylic acid ethyl ester
Conditions | Yield |
---|---|
In ethanol Heating; | 100% |
t-butyl S-3,6-diisopropylpyrazin-2-ylthiolcarbonate
cyclohexylamine
tert-butyl cyclohexylcarbamate
Conditions | Yield |
---|---|
With triethylamine In acetonitrile for 0.166667h; Ambient temperature; | 100% |
N-(1-Benzotriazolylcarbonyl)-DL-alanin
cyclohexylamine
D,L-alanine cyclohexylamide
Conditions | Yield |
---|---|
In water; acetone for 3h; Ambient temperature; | 100% |
Conditions | Yield |
---|---|
With lithium In tetrahydrofuran at 25℃; for 2h; Inert atmosphere; | 100% |
Stage #1: cyclohexylamine; benzaldehyde In methanol at 64℃; for 3h; Borch Reduction; Stage #2: With sodium cyanoborohydride In methanol; ethanol at 20 - 64℃; for 5h; Borch Reduction; | 100% |
With 1.1 wt% Pd/NiO; hydrogen In ethanol at 25℃; under 760.051 Torr; for 10h; | 98% |
cyclohexylamine
N,N-dimethyl-formamide dimethyl acetal
N,N-dimethyl-N'-cyclohexylformamidine
Conditions | Yield |
---|---|
at 60℃; | 100% |
In methanol at 25℃; for 12h; | 98% |
1.) 50 deg C, 5 h, 2.) room temperature, 12 h; | 92% |
In benzene for 1h; Heating; | 64% |
cyclohexylamine
2-Chloro-3-<α-cyano-α-(benzimidazol-2-yl)methylene>3,4-dihydroquinoxaline
1-Cyclohexyl-2-Amino-3-(benzimidazol-2-yl)pyrrolo<2,3-b>quinoxaline
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 0.666667h; Heating; | 100% |
cyclohexylamine
[3-Chloro-1H-quinoxalin-(2Z)-ylidene]-(1-methyl-1H-benzoimidazol-2-yl)-acetonitrile
1-Cyclohexyl-3-(1-methyl-1H-benzoimidazol-2-yl)-1H-pyrrolo[2,3-b]quinoxalin-2-ylamine
Conditions | Yield |
---|---|
for 0.0833333h; Heating; | 100% |
cyclohexylamine
4-dimethylamino-benzaldehyde
N-<<4-(dimethylamino)phenyl>methylene>cyclohexylamine
Conditions | Yield |
---|---|
With sodium sulfate In methanol for 4h; Ambient temperature; | 100% |
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