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:555-16-8
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inquiryItems Standard Result Appearance Light yellow crystalline powder Complies Assay 99%min
Cas:555-16-8
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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
Cas:555-16-8
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inquiryProduct description: Product name 4-Nitrobenzaldehyde CAS number 555-16-8 Assay ≥99% Appearance Light yellow powder Capacity 100mt/year Application Dye/pharmaceutical interme
Cas:555-16-8
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inquiry1, Full experience of large numbers containers loading in main Chinese seaports 2, Packing with pallet as buyer's special request 3, Best service after shipment with e-mail 4, Cargoes together with container sales service available 5, R
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inquiry4-Nitrobenzaldehyde Appearance : White or pale yellow prism crystal Structural formula: Content: ≥99.0% Moisture: ≤0.5% Melting point:
Cas:555-16-8
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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
Colorcom is a global leader in industrial chemical manufacturing and is continuously innovating and transforming to exceed client expectations and industry standards. Colorcom prides itself on superior customer and technical focus, while focusing on
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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inquiryName:4-nitro-Benzaldehyde CAS NO:555-16-8 Grade:This product is an intermediate for organic synthesis of dyes and medicine. It is used to produce nitrophenylbutenone in the pharmaceutical industry. P-nitrobenzaldehyde is an important intermediate f
Cas:555-16-8
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inquiryProduct name: p-nitrobenzaldehyde 4-Nitrobenzaldehyde Basic information Product Name: 4-Nitrobenzaldehyde Synonyms: 4-NITROBENZALDEHYDE;4-FORMYLNITROBENZENE;AKOS BBS-00003206;P-NI
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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:555-16-8
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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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inquiryp-nitrobenzaldehyde Molecular formula: C7H5NO3 CAS NO.: 555-16-8 Appearance: light yellow crystalline powder Content: 99% min GC. Appearance:light yellow crystalline powder Storage:Store in cool
Cas:555-16-8
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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
Cas:555-16-8
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inquiryWe are the manufacturers and suppliers of API in China, and warehouse in Germany and USA of California, which can quickly and safely deliver to your address 1.High quality and competitive price. 2.Free sample for your evaluation. 3.Promptly delivery
Cas:555-16-8
Min.Order:10 Gram
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inquiry4-Nitrobenzaldehyde CAS:555-16-8 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic interme
Cas:555-16-8
Min.Order:1 Gram
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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
Cas:555-16-8
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inquiryHebei Mojin Biotechnology Co., Ltd, Our company is a professional chemical raw materials and chemical reagents research and development production enterprises. We have several production line,So we can control the lowest price. We also have several
Cas:555-16-8
Min.Order:25 Gram
FOB Price: $90.0 / 100.0
Type:Trading Company
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
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
Lorcaserin(856681-05-5)is an orally administered agent and a selective 5-HT2C receptor agonist for the treatment of obesity. It had been approved for marketing in US by FDA on 27 June in 2012. In clinical studies, lorcaserin h
Cas:555-16-8
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inquiryOur advantage: high quality with competitive price High quality standard: BP/USP/EP Enterprise standard All purity customized Fast and safe delivery We have reliable forwarder who can help us deliver our goods more fast and safe. We have s
Hangzhou 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:555-16-8
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inquiryFactory direct sales, accept customization. 4-Nitrobenzaldehyde is a benzaldehyde with a nitro group in the para position. It is used as a reagent in decarboxylative aldol reactions that are catalyzed by lipases and proteases in organic co-solvent m
Company Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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
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
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:555-16-8
Min.Order:10 Gram
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inquiryProduct name: 4-Nitrobenzaldehyde CAS No.:555-16-8 Molecule Formula:C7H5NO3 Molecule Weight:151.12 Purity: 99.0% Package: 25kg/drum Description:White to pale yellow powder Manufacture Standards:Enterprise Standard TESTING ITEMS
Cas:555-16-8
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With bis(2,2'-bipyridyl) copper(II) permanganate In dichloromethane for 1.5h; Ambient temperature; | 100% |
With pyridine chromium peroxide In benzene for 0.2h; Heating; | 100% |
With tert.-butylhydroperoxide; polystyrene-bound phenylselenic acid In tetrachloromethane for 5h; Heating; | 100% |
Conditions | Yield |
---|---|
With [NO(1+)*18-crown-6*H(NO3)2(1-)]; silica gel In dichloromethane at 20℃; for 0.0833333h; | 100% |
With sulphated zirconia In acetonitrile at 60℃; for 0.6h; Microwave irradiation; | 100% |
With beta zeolite modified with chlorosulphonic acid (28 wtpercent) In ethanol at 50℃; for 0.5h; | 100% |
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; dimethyl selenoxide In acetonitrile for 5h; Heating; | 100% |
With 2-dimethylamino-N,N-dimethylaniline N-oxide In acetonitrile at 25℃; for 24h; Oxidation; | 97% |
With potassium hydrogencarbonate; dimethyl sulfoxide for 0.0333333h; Microwave irradiation; | 97% |
4-nitrophenyl-1,3-dithiane
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With silica gel; ferric nitrate In hexane at 50℃; for 0.166667h; | 100% |
With ferric nitrate Ambient temperature; | 98% |
With 1-benzyl-4-aza-1-azoniabicyclo[2.2.2]octane tribromide In methanol; dichloromethane at 20℃; for 0.05h; | 98% |
4-nitrobenzyl trimethylsilyl ether
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With dinitrogen tetraoxide; ferric nitrate In dichloromethane at 20℃; for 1h; Oxidation; | 100% |
With nitrogen dioxide at 20℃; for 1h; | 100% |
With n-butyltriphenylphosphonium peroxodisulfate In acetonitrile for 0.5h; Heating; | 97% |
4-nitrobenzaldehyde di-n-butyl acetal
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane 0 deg C to RT; | 100% |
aluminum oxide In gas at 350℃; Yield given; |
Conditions | Yield |
---|---|
With water for 1080h; | A 100% B 100% |
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With hydrogenchloride for 0.0416667h; Product distribution; Ambient temperature; pH = 4-6, regeneration of aldehyde; | 100% |
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 0℃; for 3h; | 100% |
tert-butyldimethyl-4-nitrobenzyloxysilane
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With dinitrogen tetraoxide; ferric nitrate at 20℃; for 0.5h; Oxidation; | 100% |
With tetra-N-butylammonium tribromide In acetonitrile at 20℃; for 6h; Irradiation; | 98% |
With N-hydroxyphthalimide; oxygen; cobalt(II) benzoate In acetonitrile at 20℃; for 5h; | 91% |
Conditions | Yield |
---|---|
With ozone; 1-[{4-(phenylazo)-phenyl}-azo]-2-naphthalenol In water; acetonitrile at 0℃; | 100% |
Stage #1: 4-nitrostyrene With ozone In acetone at 25℃; Stage #2: With water In acetone at 25℃; | 84% |
With ruthenium trichloride; [bis(acetoxy)iodo]benzene In dichloromethane; water at 30℃; for 2.5h; | 83.5% |
4-nitrobenzyl chloride
di(p-tolyl) sulfoxide
A
di-(p-tolyl)sulfane
B
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With per-rhenic acid In toluene for 17h; Reagent/catalyst; Time; Reflux; | A 96% B 99% |
Conditions | Yield |
---|---|
With methanol; potassium permanganate In ethyl acetate at 25℃; for 16h; Solvent; | 99% |
Conditions | Yield |
---|---|
With water at 20 - 80℃; for 24h; Inert atmosphere; | 98.1% |
With carbon tetrabromide In water; acetonitrile at 80℃; for 2h; | 97% |
indium(III) chloride In methanol; water for 0.833333h; Heating; | 95% |
Conditions | Yield |
---|---|
With oxygen; 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt In tetrahydrofuran Ambient temperature; laccase from Coriolus versicolor; | 98% |
With dihydrogen peroxide In acetonitrile at 50 - 80℃; for 24h; Reagent/catalyst; | 95% |
With nickel-doped graphene carbon nitride nanoparticles; air In ethanol at 25℃; for 8h; Irradiation; Green chemistry; | 95% |
Conditions | Yield |
---|---|
With dipotassium hydrogenphosphate; dimethyl selenoxide; tetrabutylammomium bromide In 1,2-dimethoxyethane for 4h; Heating; | 98% |
With bismuth(III) nitrate; tetrabutyl ammonium fluoride at 100℃; for 2.7h; | 95% |
With 1-dodecyl-3-methylimidazolium iron chloride; periodic acid at 30℃; for 2.5h; | 90% |
Conditions | Yield |
---|---|
With n-butyltriphenylphosphonium peroxodisulfate In acetonitrile for 2h; Heating; | 98% |
With silica-OSO3H; silica gel In toluene at 60 - 70℃; for 1h; | 98% |
With iron(III) p-toluenesulfonate hexahydrate In water for 0.666667h; Reflux; | 98% |
tri-p-tolylphosphine sulfide
2-methyl-3-p-nitrophenyloxaziridine
A
(E)-N-methyl-1-(4-nitrophenyl)methanimine
B
tri(4-methylphenyl)phosphine oxide
C
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
In chloroform-d1 at 40℃; for 72h; Rate constant; Product distribution; Mechanism; Irradiation; | A 53% B 98% C 31% |
Conditions | Yield |
---|---|
With potassium permanganate; 1-n-butyl-3-methylimidazolim bromide at 20℃; for 0.15h; Ionic liquid; chemoselective reaction; | 98% |
With copper(II) choride dihydrate; water In acetonitrile at 75℃; for 2.5h; | 98% |
With bis(1-CH2Ph-3,5,7-3N-1-N(1+)tricyclo[3.3.1.13,7]decaneS2O8 In acetonitrile for 0.5h; Oxidation; Heating; | 97% |
2-(4-nitrophenyl)-1,3-dithiolane
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With silica gel; copper(II) nitrate In tetrachloromethane for 1h; Ambient temperature; | 98% |
With ferric nitrate for 0.0111111h; Irradiation; microwave; | 97% |
Stage #1: 2-(4-nitrophenyl)-1,3-dithiolane In ethanol at 20℃; Stage #2: With water In ethanol at 20℃; | 96% |
Conditions | Yield |
---|---|
With tungsten(VI) chloride In dichloromethane for 7h; Ambient temperature; | 98% |
With tetrachlorosilane In dichloromethane at 20℃; for 0.666667h; | 88% |
perchloric acid In ethanol; water at 25 - 30℃; for 1h; | 88% |
Conditions | Yield |
---|---|
With quinolinium dichromate(VI) In acetonitrile for 1.75h; Heating; | 98% |
With potassium permanganate; silica gel In water at 20℃; for 0.416667h; | 98% |
With water; silica gel; bis(trimethylsilyl)chromate In chloroform for 0.416667h; Heating; | 97% |
2-(4-nitrophenyl)-1,3-oxathiolane
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With bromine; dimethyl sulfoxide In chloroform at 20℃; for 0.0666667h; | 98% |
With bromine; silica gel In dichloromethane at 20℃; for 0.166667h; | 98% |
Stage #1: 2-(4-nitrophenyl)-1,3-oxathiolane In ethanol at 20℃; for 0.166667h; Stage #2: With water In ethanol at 20℃; for 0.333333h; | 98% |
Conditions | Yield |
---|---|
With aluminium trichloride; 1-benzyl-1-aza-4-azoniabicyclo<2.2.2>octane periodate at 20℃; for 0.333333h; | 98% |
With dihydrogen peroxide; vanadia; ammonium bromide In dichloromethane; water at 0 - 5℃; for 2h; | 96% |
With cetyl(trimethyl)-ammonium tribromide In dichloromethane at 0 - 5℃; for 0.5h; | 90% |
With ammonium heptamolybdate; dihydrogen peroxide; ammonium bromide; perchloric acid In dichloromethane; water at 0 - 5℃; for 0.333333h; | 77% |
Conditions | Yield |
---|---|
With bismuth(III) nitrate; silica gel In acetone for 0.5h; | 98% |
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; water; silica gel In dichloromethane at 20℃; for 2h; | 92% |
With potassium permanganate; silica gel In water at 20℃; for 0.416667h; | 90% |
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With silica-OSO3H; silica gel In toluene at 60 - 70℃; for 1h; | 98% |
With tetrachlorosilane; silica gel In toluene at 60 - 70℃; for 0.75h; | 95% |
With potassium sulfate; potassium hydrogensulfate; potassium peroxomonosulfate; aluminium trichloride In acetonitrile Heating; |
4-nitrostilbene
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; osmium(VIII) oxide; [bis(acetoxy)iodo]benzene; water In tetrahydrofuran at 25℃; for 9h; Inert atmosphere; | 98% |
6-N-(4'-nitrobenzylidene)aminodeoxyvasicinone
A
4-nitrobenzaldehdye
B
7-amino-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one
Conditions | Yield |
---|---|
In ethanol at 80℃; for 1.5h; | A 92% B 98% |
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With dihydrogen peroxide In acetonitrile at 80℃; for 18h; Catalytic behavior; | 98% |
nitromethane
4-nitrobenzaldehyde dimethyl acetal
A
1-nitro-4-[(E)-2-nitroeth-1-enyl]benzene
B
4-nitrobenzaldehdye
Conditions | Yield |
---|---|
With water at 20 - 80℃; for 24h; Henry reaction; Inert atmosphere; | A 97.7% B 2.3% |
2-methyl-1H-indole
4-nitrobenzaldehdye
bis-(2-methyl-indol-3-yl)-(4-nitro-phenyl)-methane
Conditions | Yield |
---|---|
at 100℃; for 2h; Friedel Crafts alkylation; neat (no solvent); | 100% |
With bismuth(III) vanadate In neat (no solvent) at 80℃; for 0.166667h; Biginelli Pyrimidone Synthesis; Green chemistry; | 98% |
In neat (no solvent) at 20℃; for 0.0833333h; Green chemistry; chemoselective reaction; | 97% |
Conditions | Yield |
---|---|
With sulphated zirconia at 0℃; for 5h; regioselective reaction; | 100% |
With poly(4-vinylpyridine)-supported sulfuric acid In dichloromethane at 20℃; for 0.166667h; Green chemistry; chemoselective reaction; | 100% |
With SBA-15-Ph-PrSO3H at 20℃; for 1h; Reagent/catalyst; Green chemistry; | 100% |
ethyl acetoacetate
4-nitrobenzaldehdye
urea
ethyl 6-methyl-4-(4-nitrophenyl)-2-oxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxylate
Conditions | Yield |
---|---|
With 1-methylimidazole based ionic liquid terminated dendritic moiety prepared from 2,4,6-trichloro-1,3,5-triazine and 1,3-diaminopropane immobilized on 3-aminopropyltriethoxysilane functionalized bentonite In ethanol; water at 50℃; for 3h; Biginelli Pyrimidone Synthesis; Green chemistry; | 100% |
With composite of cross-linked chitosan beads and a cyclodextrin nanosponge In water for 0.25h; Biginelli Pyrimidone Synthesis; Sonication; Green chemistry; | 100% |
With guanidine In neat (no solvent) at 80℃; for 2h; Biginelli Pyrimidone Synthesis; | 99% |
1-amino-naphthalene
4-nitrobenzaldehdye
N-(napht-1-yl)-N-(p-nitrobenzylidene)amine
Conditions | Yield |
---|---|
for 24h; Ambient temperature; | 100% |
In ethanol | 85% |
With ethanol |
Conditions | Yield |
---|---|
With C57H78N12; copper(II) acetate monohydrate In methanol; dichloromethane for 72h; Henry reaction; Inert atmosphere; | 100% |
With polymer supported 4-DMAP at 20℃; for 0.333333h; Reagent/catalyst; Henry Nitro Aldol Condensation; | 100% |
With P(i-PrNCH2CH2)3N; magnesium sulfate for 0.0833333h; Ambient temperature; | 99% |
propylene glycol
4-nitrobenzaldehdye
4-methyl-2-(4-nitro-phenyl)-[1,3]dioxolane
Conditions | Yield |
---|---|
With cyclohexane at 105℃; for 1h; Dean-Stark; | 100% |
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide In ethyl acetate at 20℃; | 93% |
With toluene-4-sulfonic acid; benzene Unter Entfernen des entstehenden Wassers.; |
Conditions | Yield |
---|---|
With pyridine In ethanol for 1.75h; Knoevenagel condensation; Inert atmosphere; Reflux; | 100% |
With ammonium acetate for 0.0666667h; Irradiation; | 95% |
Stage #1: malonic acid; 4-nitrobenzaldehdye With piperidine; pyridine Knoevenagel-Doebner reaction; Reflux; Stage #2: With hydrogenchloride In water Cooling with ice; optical yield given as %de; | 95% |
1,2,4-trimethoxy-benzene
4-nitrobenzaldehdye
1,1'-[(4-nitrophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)
Conditions | Yield |
---|---|
With o-benzenedisulfonimide at 130℃; for 0.25h; Friedel Crafts alkylation; | 100% |
With air; iodine In toluene at 20℃; for 72h; Friedel Crafts alkylation; | 99% |
With niobium pentachloride In dichloromethane at 0 - 20℃; for 24h; Friedel-Crafts Alkylation; | 98% |
N-methylhydroxyamine hydrochloride
4-nitrobenzaldehdye
N-(p-nitrobenzylidene)methylamine N-oxide
Conditions | Yield |
---|---|
With 3 A molecular sieve at 20℃; for 0.25h; | 100% |
With sodium hydroxide; silica gel at 20℃; for 0.166667h; | 96% |
With sodium hydrogencarbonate In dichloromethane for 0.1h; microwave irradiation; | 95% |
4-nitrobenzaldehdye
p-toluidine
N-(4-nitrobenzylidene)-4-methylaniline
Conditions | Yield |
---|---|
for 24h; Ambient temperature; | 100% |
100% | |
With montmorillonite at 20℃; for 0.0666667h; Neat (no solvent); | 98% |
4-nitrobenzaldehdye
4-methoxy-aniline
4-methoxy-N-(4-nitrobenzylidene)aniline
Conditions | Yield |
---|---|
at 50℃; for 24h; | 100% |
for 6h; Molecular sieve; Reflux; | 100% |
In ethanol for 3h; Reflux; | 95% |
Conditions | Yield |
---|---|
at 20℃; under 750.06 Torr; Solid phase reaction; gas-solid reaction; | 100% |
With water | |
In ethanol at 50℃; | |
In tetrahydrofuran; ethanol at 20℃; for 12h; Inert atmosphere; | |
In ethanol at 20℃; for 12h; |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene at 143℃; for 2h; Dean-Stark; | 100% |
With cyclohexane at 105℃; for 1h; Dean-Stark; | 100% |
With p-toluenesulfonic acid monohydrate In toluene for 4h; Reflux; | 100% |
4-nitrobenzaldehdye
4-nitro-aniline
N-(4-nitrobenzylidene)-4-nitroaniline
Conditions | Yield |
---|---|
at 60℃; for 2h; | 100% |
at 83 - 85℃; | 100% |
With sulfuric acid In neat (no solvent) Microwave irradiation; Sealed tube; Green chemistry; | 72% |
4-nitrobenzaldehdye
phosphonic acid diethyl ester
diethyl (hydroxy(4-nitrophenyl)methyl)phosphonate
Conditions | Yield |
---|---|
With magnesium oxide for 0.17h; | 100% |
With {(μ-η5:η1):η1-2-[(2,6-Me2C6H3)NCH2](C4H3N)SmN(SiMe3)2}2 In toluene at 20℃; for 0.166667h; Inert atmosphere; | 99% |
With [(μ-η5:η1):η1:η1-3-(2-C4H3NCH=NCH2CH2)C8H5N]Yb3(μ3-O)-(μ2-Cl)2(THF)2[N(SiMe3)2] In neat (no solvent) at 20℃; for 0.166667h; Inert atmosphere; | 99% |
4-nitrobenzaldehdye
acetone
1-(4-nitrophenyl)-1-hydroxy-3-butanone
Conditions | Yield |
---|---|
With Zn(2+)-(TyrOEt)2 In water at 40℃; for 24h; pH 7; | 100% |
With sodium hydroxide at 25℃; for 0.166667h; | 100% |
With Fe(OH)3/Fe3O4 at 50℃; for 3h; | 99% |
Conditions | Yield |
---|---|
at 150℃; for 1h; Knoevenagel condensation; | 100% |
In various solvent(s) at 20℃; for 3h; Knoevenagel condensation; | 100% |
hydrotalcite structure integrating fluoride ions In acetonitrile at 25℃; for 1.5h; Conversion of starting material; Knoevenagel Condensation; | 100% |
Conditions | Yield |
---|---|
With Nafion-H at 150℃; for 0.5h; Microwave irradiation; | 100% |
With boron trifluoride monohydrate at 50℃; for 2h; Sealed tube; | 98% |
With trifluorormethanesulfonic acid at 50℃; for 0.583333h; | 96% |
Conditions | Yield |
---|---|
With hydrazine hydrate In ethanol; water at 80℃; for 1h; chemoselective reaction; | 100% |
With NiRh3; hydrogen In ethyl acetate at 20℃; for 12h; Mechanism; Reagent/catalyst; Solvent; chemoselective reaction; | 99% |
With hydrogen In ethanol; water at 25℃; under 11251.1 Torr; for 6h; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate; 1-(phenyl-2-ethyl)-7-methyl-3,5-N,N-diethylaminocarbonyl-4,7-dihydropyrrolo<2,3-b>pyridine In acetonitrile at 60℃; for 1h; Product distribution; Rate constant; reduction of other benzaldehydes and ketones and carbon carbon double bonds; | 100% |
With magnesium(II) perchlorate; model of NADH grafted on silica matrix In acetonitrile at 65℃; for 120h; Product distribution; also with methyl benzoylformiate; varied lenght of chain, between reagent and surface of the support, reaction time, proportion of reagent/p-NBA; | 100% |
With magnesium(II) perchlorate; polymer-bound NADH (2a) In acetonitrile; benzene at 80℃; for 120h; Further byproducts given; | 100% |
Conditions | Yield |
---|---|
With pyridine; hydroxylamine hydrochloride In ethanol | 100% |
With N-hydroxyphthalimide In water at 90℃; for 3h; Sealed tube; | 98% |
With perchloric acid; ethyl acetohydroximate In dichloromethane; water at 20℃; for 24h; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
With [(ImDippN)Th{N(SiMe3)2}3] In benzene-d6 at 20℃; for 24h; Reagent/catalyst; Time; | 100% |
With Mg[iPr2NC{N-2,6-Me2-C6H3}2]2 In toluene at 25℃; for 12h; Reagent/catalyst; Tishchenko-Claisen Dismutation; Inert atmosphere; | 91% |
With phenylmethanethiol; phenylmagnesium bromide In tetrahydrofuran; diethyl ether at 65℃; for 18h; Tishchenko reaction; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With sodium perborate In acetic acid for 1.5h; steam bath; | 100% |
With phosphate-buffered silica gel supported KMnO4 In cyclohexane at 65℃; | 100% |
With [Cu2C6H4(CHNCH2CH2N(CH2C5H4N)2)2](2+)*2ClO4(1-)=C36H38Cu2N8(ClO4)2; oxygen In acetone at -90.16℃; | 100% |
trimethylsilyl cyanide
4-nitrobenzaldehdye
2-(4-nitrophenyl)-2-[(trimethylsilyl)oxy]acetonitrile
Conditions | Yield |
---|---|
With 2Zn(2+)*10H2O*3C10H8N2*2H(1+)*Co2Mo10H4O38(6-) In neat (no solvent) at 25℃; for 7h; Reagent/catalyst; Inert atmosphere; | 100% |
With C42H50Mg2N4 In benzene-d6 at 25℃; Glovebox; Inert atmosphere; | 99% |
With cobalt incorporated covalent organic framework of 2,3-dihydroxyterephthalohydrazide with triformylphloroglucinol (NUS-51-Co) In dichloromethane at 24.84℃; for 10h; Catalytic behavior; | 99% |
morpholine
4-nitrobenzaldehdye
4,4'-((4-nitrophenyl)methylene)dimorpholine
Conditions | Yield |
---|---|
With copper(II) bis(trifluoromethanesulfonate) In water at 20℃; for 0.0333333h; | 100% |
In benzene for 2h; Heating; | 97% |
In benzene Reflux; | 90% |
With potassium carbonate In dichloromethane at 20℃; | 82% |
pyrrole
4-nitrobenzaldehdye
2,2'-[(4-nitrophenyl)methylene]bis(1H-pyrrole)
Conditions | Yield |
---|---|
With hydrogenchloride In water at 20℃; for 2h; | 100% |
With tetramethyl-tetra-3,4-pyridinoporphyrazinato copper(II) methyl sulfate In water at 20℃; | 98% |
With hydrogenchloride In water at 20℃; for 2h; | 97% |
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