Quick Details ProName: 1,2,4,5-Benzenetetracarboxylic anhydri... CasNo: 89-32-7 Molecular Formula: C10H2O6 Appearance: white crystalline powder Application: manufacturing polyimide film,High-perf... DeliveryTi
Cas:89-32-7
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inquiryAs 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:89-32-7
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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:89-32-7
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inquiryProduct description: Product name Pyromellitic dianhydride (PMDA) CAS number 89-32-7 Assay ≥99% Appearance Yellowish to off-white crystalline powder Capacity 500mt/year Applicat
Cas:89-32-7
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inquiryCAS No.: 89-32-7 Other Names: PMDA MF: C10H2O6 EINECS No.: 201-898-9 Place of Origin: China (Mainland)
Cas:89-32-7
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inquiryHebei yanxi chemical co., LTD is a professional research, development and production Cyromazine、lead diacetate trihydrate /Lead acetate trihydrateC、 2-phenylacetamide 、 4-Aminophenyl-1-phenethylpiperidine 、Citric acid monohydrate 、 Citric acid/c
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inquiryT he company has advanced technology, as well as a large number of excellent R & D team, to provide customers from the grams to one hundred kilograms and tons of high-quality products, competitive prices and quality service Appearance:white
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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inquiryChemwill Asia co.,Ltd is one of the leading manufacturer in CHINA. Product quality, process, price and service Pyromellitic Dianhydride CAS 1143-72-2 PMDA IN Stock 1,2,4,5-Benzenetetracarboxylic anhydride CAS 1143-72-2 1143-72-2 CAS 1143-7
Cas:89-32-7
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inquiry1,2,4,5-Benzenetetracarboxylic anhydride Basic information Product Name: 1,2,4,5-Benzenetetracarboxylic anhydride Synonyms: 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-dianhydride;1,2,4,5benz
Cas:89-32-7
Min.Order:1 Gram
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inquiryProduct Name Pyromellitic Dianhydride Synonyms 1,2,4,5-Benzenetetracarboxylic 1,2:4,5-dianhydride;1,2,4,5benzenetetracarboxylic1,2:4,5dianhydride;1,2,4,5-benzenetetracarboxylic1,2:4,5-dianhydride;1,2,4,5-B
Cas:89-32-7
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inquiryAdvantages: Hubei XinRunde Chemical Co., Ltd is a renowned pharmaceutical manufacturer. We can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. Never stop striving to offer our best service is
Cas:89-32-7
Min.Order:1 Kilogram
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Type:Other
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
Price, service, company and transport advantage: 1.place of origin china with super quality by reasonable price. 2.fast delivery by safe express way to all the country. 3.has a number of highly qualified engineers and experts to p
Cas:89-32-7
Min.Order:10 Gram
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Type:Trading Company
inquiryTriumph has the complete production of G- KG - MT service chain,we can make the new technology into productivity quickly in the research and development of new products. Main Service 1.Own made fine chemical products 2.Out sourcing and quality c
Cas:89-32-7
Min.Order:100 Metric Ton
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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:89-32-7
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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:89-32-7
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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
Cas:89-32-7
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Type:Lab/Research institutions
inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
Cas:89-32-7
Min.Order:4 Kilogram
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Type:Lab/Research institutions
inquiryZibo 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:89-32-7
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirySuperior quality Appearance:white powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceutical Intermediates Transportation:as pe
Cas:89-32-7
Min.Order:1 Kilogram
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Type:Trading Company
inquiryProduct 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:89-32-7
Min.Order:1 Kilogram
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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service and h
Cas:89-32-7
Min.Order:0
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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 custom synthe
Cas:89-32-7
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inquiryHebei Lead Bio-Chemicals Co., Ltd. established in 2006, devolved in resurching, manufacturing and supplying of pharmaceuticals,food ingredients, cosmetics,health care products, Chinese herb, plant extracts and some fine chemicals,is one of leading gr
Cas:89-32-7
Min.Order:0
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Type:Manufacturers
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
Cas:89-32-7
Min.Order:0
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Type:Manufacturers
inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
high purity,in stock Package:25kg/drum,or as per customers'demand Application:API,or Intermediates,fine chemicals Transportation:air,sea,courier
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Cas:89-32-7
Min.Order:100 Gram
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Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With acetic anhydride for 3h; Reflux; | 97% |
With 2,6-bis[(2,2,6,6-tetramethylpiperidin-1-yl)methyl]phenylboronic acid In propyl cyanide for 12h; Reflux; | 90% |
2,6-bis[(2,2,6,6-tetramethylpiperidin-1-yl)methyl]phenylboronic acid In butryonitrile for 12h; Reflux; | 90% |
Conditions | Yield |
---|---|
at 450 - 565℃; Leiten im Gemisch mit Luft ueber Vanadium(V)-oxid; | |
With oxygen at 398℃; Gas phase; |
1,4-diethyl-2,5-dimethyl-benzene
Pyromellitic dianhydride
Conditions | Yield |
---|---|
at 450 - 565℃; Leiten im Gemisch mit Luft ueber Vanadium(V)-oxid; |
Conditions | Yield |
---|---|
durch trockne Destillation; |
4,5-dimethylphthalic anhydride
A
phthalic anhydride
B
4-methylphthalic anhydride
C
3-methylphthalic acid anhydride
D
Pyromellitic dianhydride
Conditions | Yield |
---|---|
With vanadia at 400℃; Product distribution; effect of temperature on gas-phase oxidation; |
2,5-dimethylterephthalic acid
A
maleic anhydride
B
Pyromellitic dianhydride
C
1,2,4-benzene tricarboxylic acid
D
trimellitic Anhydride
Conditions | Yield |
---|---|
With vanadia at 400℃; Product distribution; effect of temperature on gas-phase oxidation; |
2,4-dimethylisophthalic acid
A
Pyromellitic dianhydride
B
1,2,4-benzene tricarboxylic acid
C
trimellitic Anhydride
Conditions | Yield |
---|---|
With vanadia at 400℃; Product distribution; effect of temperature on gas-phase oxidation of methyl-substituted carboxylic acids and anhydrides; |
Pyromellitic dianhydride
Conditions | Yield |
---|---|
at 270 - 300℃; |
Conditions | Yield |
---|---|
at 270 - 300℃; |
Conditions | Yield |
---|---|
bei der trocknen Destillation; |
1,2,4,5-tetramethylbenzene
A
1,2,4,5-benzenetetracarboxylic acid
B
Pyromellitic dianhydride
Conditions | Yield |
---|---|
Stage #1: 1,2,4,5-tetramethylbenzene With oxygen; acetic acid; cobalt(II) acetate; manganese(II) acetate; 2,6-dihydroxypyrrolo[3,4-f]isoindolo-1,3,5,7(2H,6H)tetrone In water at 120℃; under 30003 Torr; for 2h; Stage #2: With acetic anhydride In water at 120 - 150℃; under 3750.38 - 30003 Torr; for 4h; Product distribution / selectivity; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aluminium chloride / 50 - 70 °C 2: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 3: 290 °C / 13 Torr View Scheme | |
Multi-step reaction with 8 steps 1: phosphorus pentoxide / 190 °C 3: 130 - 140 °C 4: amalgamated zinc; hydrochloric acid 5: phosphorus pentachloride / nachfolgend Destillation im Vakuum 6: amalgamated zinc; concentrated hydrochloric acid 7: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 8: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: nickel catalyst; tetralin / 200 - 220 °C / Hydrogenation 2: aluminium chloride / 80 °C 3: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 4: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: nickel catalyst; tetralin / 180 - 200 °C / Hydrogenation 2: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 3: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: amalgamated zinc; concentrated hydrochloric acid 2: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 3: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 2: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: aluminium chloride / 80 °C 2: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 3: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 2: 130 - 140 °C 3: amalgamated zinc; hydrochloric acid 4: phosphorus pentachloride / nachfolgend Destillation im Vakuum 5: amalgamated zinc; concentrated hydrochloric acid 6: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 7: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: phosphorus pentachloride / nachfolgend Destillation im Vakuum 2: amalgamated zinc; concentrated hydrochloric acid 3: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 4: 290 °C / 13 Torr View Scheme |
[2-oxo-2-(5,6,7,8-tetrahydro-[2]naphthyl)-ethyl]-malonic acid
Pyromellitic dianhydride
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 130 - 140 °C 2: amalgamated zinc; hydrochloric acid 3: phosphorus pentachloride / nachfolgend Destillation im Vakuum 4: amalgamated zinc; concentrated hydrochloric acid 5: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 6: 290 °C / 13 Torr View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: amalgamated zinc; hydrochloric acid 2: phosphorus pentachloride / nachfolgend Destillation im Vakuum 3: amalgamated zinc; concentrated hydrochloric acid 4: bei aufeinanderfolgender Oxydation mit sodaalkalischer und mit schwefelsaurer Permanganat-Loesung 5: 290 °C / 13 Torr View Scheme |
1,2,4,5-benzenetetracarboxylic acid
5-methyl-1,2,4-benzenetricarboxylic acid
1,2,4-benzene tricarboxylic acid
benzene-1,2-dicarboxylic acid
B
Pyromellitic dianhydride
C
3,3',4,4'-benzophenonetetracarboxylic acid
D
pyromellitic acid monoanhydride
Conditions | Yield |
---|---|
Stage #1: 1,2,4,5-benzenetetracarboxylic acid; 5-methyl-1,2,4-benzenetricarboxylic acid; 1,2,4-benzene tricarboxylic acid; benzene-1,2-dicarboxylic acid at 235 - 250℃; for 7.5 - 30h; Stage #2: With acetic anhydride In acetic acid at 120 - 170℃; under 750.075 - 4500.45 Torr; Product distribution / selectivity; |
2,4,5-tris(ethoxycarbonyl)benzoic acid
A
diethyl 1,3-dioxo-1,3-dihydroisobenzofuran-5,6-dicarboxylate
B
Pyromellitic dianhydride
Conditions | Yield |
---|---|
Heating; | A 31.8 g B n/a |
1,2,4,5-benzenetetracarboxylic acid
acetic anhydride
Pyromellitic dianhydride
Conditions | Yield |
---|---|
for 2h; Reflux; |
Pyromellitic dianhydride
Conditions | Yield |
---|---|
at 20 - 180℃; for 4h; |
1,1'-(1,2-ethanediyl)bis-(2,4,5-trimethylbenzene)
Pyromellitic dianhydride
Conditions | Yield |
---|---|
With air; V2O5-TiO2-P2O5 catalyst at 380℃; Temperature; |
Pyromellitic dianhydride
methylamine
N,-N'-Dimethylpyromellitic acid diimide
Conditions | Yield |
---|---|
at 160℃; under 600.048 Torr; Condensation; solid-gas reaction; | 100% |
Conditions | Yield |
---|---|
under 750.06 Torr; Condensation; solid-gas reaction; ring cleavage; | 100% |
[(m-aminophenylamino)-4-aminophenylmethylidene]propanedinitrile
Pyromellitic dianhydride
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one; chlorobenzene at 20 - 190℃; | 100% |
Pyromellitic dianhydride
Conditions | Yield |
---|---|
With calcium fluoride at -266.46℃; Photolysis; | 100% |
Pyromellitic dianhydride
4-hexadecylaniline
zinc diacetate
[Zn(C20H8N4((C4H9)2C6H3)3(C6H4)(C10H2N2O4)(C6H4)(C16H33))]
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide (C20H10N4((C4H9)2C6H3)3(C6H4))NH2, C10H2O6, (C16H33)NH(C6H5) (dry DMF) heated under N2 in dark for 22 h, cooled to 25°C, evapd. to dryness (reduced pressure); chromy., dissolved (CHCl3), added Zn(OAc)2 in CH3OH, heated for 30 min; washed twice (H2O), dried (anhydrous Na2SO4), solvent evapd., chromy., reprecipitated from chloroform-methanol; | 100% |
Pyromellitic dianhydride
orthoformic acid triethyl ester
1,2,4,5-benzenetetracarboxylic acid ethyl ester
Conditions | Yield |
---|---|
Stage #1: Pyromellitic dianhydride; orthoformic acid triethyl ester Stage #2: With water | 100% |
In ethanol for 4.5h; Heating; | 99.2% |
Pyromellitic dianhydride
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one at 25℃; for 2h; | 100% |
Conditions | Yield |
---|---|
Stage #1: Pyromellitic dianhydride In water at 80℃; for 1h; Inert atmosphere; Stage #2: 1,4-phenylenediamine In water at 80℃; for 4h; Inert atmosphere; | 100% |
Pyromellitic dianhydride
trimethyl orthoformate
tetramethyl 1,2,4,5-benzenetetracarboxylate
Conditions | Yield |
---|---|
In methanol for 7.5h; Heating; | 99.9% |
Conditions | Yield |
---|---|
With urea In N,N-dimethyl-formamide for 0.0666667h; microwave irradiation; | 99% |
With choline chloride; urea at 140℃; for 1h; Green chemistry; | 97% |
With formamide for 0.0333333h; microwave irradiation; | 96% |
Conditions | Yield |
---|---|
at 130 - 140℃; | 99% |
Pyromellitic dianhydride
(S)-methyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
Conditions | Yield |
---|---|
Stage #1: Pyromellitic dianhydride; (S)-methyl 3-(4-aminophenyl)-2-((tert-butoxycarbonyl)amino)propanoate With N,N-dimethyl acetamide at 20℃; for 22h; Inert atmosphere; Stage #2: With acetic anhydride; triethylamine at 80℃; for 2.5h; Inert atmosphere; | 98.3% |
Pyromellitic dianhydride
formamide
pyromellitic diimide.formamide
Conditions | Yield |
---|---|
at 210℃; for 0.25h; | 98% |
2-(2,3,4,5,6-pentafluorophenyl)ethan-1-amine
Pyromellitic dianhydride
N,N'-di(2-(perfluorophenyl)ethyl)pyromellitic diimide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 110℃; | 98% |
Conditions | Yield |
---|---|
With pyridine; acetic acid Reflux; | 98% |
With acetic acid Reflux; | |
With acetic acid at 20℃; for 13h; Reflux; |
L-phenylalanine
Pyromellitic dianhydride
N,N’-(pyromellitoyl)-bis-L-phenylalanine diacid
Conditions | Yield |
---|---|
With pyridine; acetic acid Reflux; | 98% |
With dmap In N,N-dimethyl-formamide at 140℃; for 0.166667h; Reagent/catalyst; Solvent; Sealed tube; Microwave irradiation; | 87% |
In acetic acid at 20℃; Reflux; | 86% |
Pyromellitic dianhydride
C18H31N3O
(C5H4NCH2NHCO(CH2)11)2C10H2N2O4
Conditions | Yield |
---|---|
Heating; | 98% |
Conditions | Yield |
---|---|
for 19h; Reflux; | 98% |
Conditions | Yield |
---|---|
With water for 4h; Reflux; | 96.6% |
With water | |
With alkali | |
With water at 80℃; Inert atmosphere; |
ethanol
Pyromellitic dianhydride
1,2,4,5-benzenetetracarboxylic acid ethyl ester
Conditions | Yield |
---|---|
With sulfuric acid Reflux; Molecular sieve; | 96% |
With sulfuric acid at 100℃; for 4h; | 68% |
Stage #1: ethanol; Pyromellitic dianhydride for 2h; Reflux; Stage #2: With sulfuric acid for 18h; Reflux; | 64% |
With sulfuric acid In benzene | |
With sulfuric acid |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20 - 140℃; for 4.5h; | 96% |
In N,N-dimethyl-formamide at 20 - 140℃; | 96% |
4,4'-bis[4-(4-amino-3-methylphenoxy)benzenesulfonyl]biphenyl
Pyromellitic dianhydride
4,4'-bis[4-(3-aminophenoxy)benzenesulfonyl]biphenyl
Conditions | Yield |
---|---|
Stage #1: 4,4'-bis[4-(4-amino-3-methylphenoxy)benzenesulfonyl]biphenyl; Pyromellitic dianhydride; 4,4'-bis[4-(3-aminophenoxy)benzenesulfonyl]biphenyl In N,N-dimethyl acetamide at 20℃; for 20h; Stage #2: at 120 - 250℃; for 1.16667h; Further stages.; | 96% |
Pyromellitic dianhydride
Conditions | Yield |
---|---|
In 1-methyl-pyrrolidin-2-one at 25℃; for 2h; | 96% |
In 1-methyl-pyrrolidin-2-one at 25℃; for 2h; | 95% |
Pyromellitic dianhydride
2-hydrazino-3-(p-chlorophenyl)-1,8-naphthyridine
C38H20Cl2N8O4
Conditions | Yield |
---|---|
With N,N-dimethyl-formamide for 0.05h; Microwave irradiation; | 96% |
Pyromellitic dianhydride
3-Amino-3-phenylpropionic acid
2,6-bis(3-hydroxy-3-oxo-1-phenylprop-1-yl)pyrrolo[3,4-f]isoindole-1,3,5,7(2H,6H)-tetraone
Conditions | Yield |
---|---|
In nitrobenzene at 155 - 165℃; for 1h; | 95% |
3-hydrazinyl-oxo-N-(1,3-thiazole-2-yl)-propanamide
Pyromellitic dianhydride
N-{1,3,5,7-tetraoxo-6-[2-(thiazol-2-ylcarbamoyl)acetylamino]-3,5,6,7-tetrahydro-1H-pyrrolo[3,4-f]isoindol-2-yl}-N'-thiazol-2-yl-malonamide
Conditions | Yield |
---|---|
With acetic acid for 6h; Reflux; | 95% |
Pyromellitic dianhydride
4-fluoro-2-phenethylamine
N,N'-di(2-(4-fluorophenyl)ethyl)pyromellitic diimide
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 110℃; | 95% |
Pyromellitic dianhydride
4-amino-phenol
N,N'-(pyromellitoyl)-bis-p-aminophenol
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 12h; Reflux; | 95% |
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