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
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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
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
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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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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
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
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Lower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
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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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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
2,4-Dinitrobenzoic acid cas 610-30-0Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Best quality with low price Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
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Known for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers.Appearance:White powder Storage:keep sealed and keep from direct light Package:According client's requirements Application:pharmaceutica
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
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inquiryKnown for its best quality and competitve price, this chemicals we offered is widely appreciated by our customers. Our advantages:1, High quality with competitive price:1) Standard:BP/USP/EP/Enterprise standard2) All Purity≥99%3) We are manufacturer
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inquiryAt Share Chemical Company, we scrupulously abide by our policy of “Excellent Quality at a Reasonable Price”. We strive to satisfy all of our customers by providing the finest quality products supported by the finest in customer servi
United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 2,4-DINITROBENZOIC ACID, CAS:610-30-0 with the most competitive price and the best qu
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1.We are specializing in providing customers with complete chemical raw materials.2.Superior quality, moderate price & quick delivery.3. Extensive international cooperation experience.4. Outstanding communication skills. Application:contact us for de
CFTC?PharmaChem?is?a?service?based?company?in?China,?a?pharmachem?division?of?Changzhou?Foreign?Trade?Corp.,supplying?raw?materials,?intermediates,?APIs?and?fine?chemicals?for?the?pharmaceutical?and?specialty?chemical?industries?worldwide. Applicatio
Manufacturer,strong R&D,professional team Storage:Store in a cool, dry place. Store in a tightly closed container. Package:according to your requirement Application:ZhiShang Chemical is owned by ZhiShang Group, is a professional new-type chemicals en
high purity Application:Drug intermediates Materials intermediates and active molecules
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With 2-(methoxymethoxy)ethanol; trimethylantimony at 50℃; for 4.33333h; Temperature; | 97% |
Conditions | Yield |
---|---|
With dihydrogen peroxide In water at 60℃; for 0.5h; Temperature; Sonication; | 96.3% |
With potassium permanganate; water; magnesium sulfate at 75℃; for 3h; pH=7; | 90.7% |
With cobalt(II) acetate; ozone; acetic acid at 30℃; Product distribution; Equilibrium constant; Further Variations:; Temperatures; Reagents; | 73.8% |
2,4-dinitrotoluene
acetic acid
B
2,4-dinitrobenzaldehyde
C
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With oxygen; ozone at 29.85℃; for 2.5h; Kinetics; Further Variations:; Temperatures; | A 61% B 6% C 28% |
N-((5R)-2c-hydroxy-3,3-dimethyl-4t,7-dioxo-(5rH)-4λ4-thia-1-aza-bicyclo[3.2.0]hept-6t-yl)-2-phenyl-acetamide
2,4-dinitrobenzoyl chloride
A
N-[(5R)-2ξ-(2,4-dinitro-benzoyloxy)-3,3-dimethyl-4t,7-dioxo-(5rH)-4λ4-thia-1-aza-bicyclo[3.2.0]hept-6t-yl]-2-phenyl-acetamide
B
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran; benzene | A n/a B 60% |
A
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With ammonium nitrate; nitric acid Reflux; | A 31% B 57.2% |
Conditions | Yield |
---|---|
With perhydrodibenzo-18-crown-6; potassium permanganate In benzene at 20℃; for 5h; Reagent/catalyst; Solvent; | 53.86% |
Conditions | Yield |
---|---|
With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; laccase from Trametes versicolor; oxygen In water at 20℃; for 144h; Enzymatic reaction; | 30% |
With silver(I) acetate; acetic acid | |
With silver nitrate; acetic acid |
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sulfuric acid |
2-nitro-4-nitroso-benzoic acid
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With nitric acid |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid |
Conditions | Yield |
---|---|
With sulfuric acid; nitric acid | |
With sulfuric acid; nitric acid im Druckrohr; |
Conditions | Yield |
---|---|
(i) PhLi, (ii) /BRN= 1900390/; Multistep reaction; |
ortho-nitrobenzoic acid
A
2,5-dinitrobenzoic acid
B
2,3-di-nitrobenzoic acid
C
2,6-dinitrobenzoic acid
D
1,2-Dinitrobenzene
E
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With nitric acid; dinitrogen pentoxide at 25℃; Product distribution; addition of nitronium trifluoromethanesulphonate; |
2,4-dinitrotoluene
A
2,4-dinitrobenzaldehyde
B
2,4-dinitrobenzyl alcohol
C
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With 1,4-dihydronicotinamide adenine dinucleotide; rat liver microsomal and cytosol proteins; NAD In water; acetone at 37℃; Product distribution; phosphate buffer, pH = 7.4; besides of NAD, NADH add of NADP, NADH; add of inhibitor: hydralazine; |
Conditions | Yield |
---|---|
With potassium hydroxide In water; dimethyl sulfoxide at 25℃; Mechanism; Rate constant; Equilibrium constant; |
2,4-dinitro-benzoic acid phenyl ester
A
2,4-dinitrobenzoic acid
B
phenol
Conditions | Yield |
---|---|
With water; 1H-imidazole In acetonitrile at 40℃; Rate constant; | |
With o-iodosobenzoic acid; water In acetonitrile at 18 - 45℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); determination of catalytic effect of iodosobenzoic acid; |
4-nitrophenyl 2,4-dinitrobenzoate
A
4-nitro-phenol
B
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With water; 1H-imidazole In acetonitrile at 40℃; Rate constant; | |
With o-iodosobenzoic acid; water In acetonitrile at 18 - 45℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); determination of catalytic effect of iodosobenzoic acid; |
Conditions | Yield |
---|---|
With dihydrogen peroxide; potassium carbonate In water; toluene Yield given; |
4-nitrobenzaldehdye
A
2,4-dinitrobenzaldehyde
B
2,4-dinitrobenzoic acid
C
4-nitro-benzoic acid
Conditions | Yield |
---|---|
With nitric acid; dinitrogen pentoxide at 35℃; Product distribution; Kinetics; Mechanism; other temperature, also with nitronium trifluoromethanesulfonate in nitric acid, relative reactivities of the investigated aldehydes; |
2,4-Dinitro-benzoic acid p-tolyl ester
A
p-cresol
B
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With water; 1H-imidazole In acetonitrile at 40℃; Rate constant; | |
With o-iodosobenzoic acid; water In acetonitrile at 18 - 45℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); determination of catalytic effect of iodosobenzoic acid; |
2,4-Dinitro-benzoic acid 4-chloro-phenyl ester
A
4-chloro-phenol
B
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With water; 1H-imidazole In acetonitrile at 40℃; Rate constant; | |
With o-iodosobenzoic acid; water In acetonitrile at 18 - 45℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); determination of catalytic effect of iodosobenzoic acid; |
2,4-Dinitro-benzoic acid 4-cyano-phenyl ester
A
4-cyanophenol
B
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With water; 1H-imidazole In acetonitrile at 40℃; Rate constant; | |
With o-iodosobenzoic acid; water In acetonitrile at 18 - 45℃; Kinetics; Mechanism; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); determination of catalytic effect of iodosobenzoic acid; |
2,4-dinitrobenzoyl chloride
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With 2,3,5-trimethyl-pyridine In water; acetonitrile at 16 - 35℃; Kinetics; |
N-(2,4-dinitrobenzoyl)imidazole
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With 1H-imidazole; potassium chloride In water; acetonitrile at 25 - 50℃; Kinetics; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); |
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With hydrogenchloride; sodium chloride In water; acetonitrile at 15 - 35℃; Kinetics; Thermodynamic data; ΔH(excit.), ΔS(excit.), ΔG(excit.); |
2-Chlor-5,7-dinitro-tropon
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With sodium hydroxide |
(1S)-1-[(2R)-oxiran-2-yl]hexan-1-ol
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran Ambient temperature; several hours; | 99.3% |
2,4-dinitrobenzoic acid
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
Conditions | Yield |
---|---|
In neat (no solvent) at 30℃; Inert atmosphere; Schlenk technique; Glovebox; chemoselective reaction; | 99% |
2,4-dinitrobenzoic acid
2,4-dinitrobenzoyl chloride
Conditions | Yield |
---|---|
With thionyl chloride In 1,2-dichloro-ethane for 2h; Heating; | 98.8% |
With thionyl chloride | |
With thionyl chloride; chloroform |
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In chlorobenzene at 80℃; for 1.5h; Mitsunobu esterification; | 98% |
cis-bicyclo[3.3.0]octan-endo-2-o1
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
Stage #1: 2,4-dinitrobenzoic acid; diisopropyl-carbodiimide In dichloromethane at 20℃; for 0.5h; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; | 97% |
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; |
Conditions | Yield |
---|---|
Stage #1: 1,3-di-tert-butylcarbodiimide; 2,4-dinitrobenzoic acid In dichloromethane at 20℃; for 0.5h; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; | 95% |
Conditions | Yield |
---|---|
With silver carbonate In dimethyl sulfoxide at 120℃; for 16h; | 94% |
With copper(l) iodide; triethylamine In dimethyl sulfoxide at 120℃; under 760.051 Torr; for 20h; Inert atmosphere; Schlenk technique; | 67% |
In water at 172.5℃; Rate constant; Mechanism; Thermodynamic data; kinetics; ΔH(excit.), ΔS(excit.); other substituted dinitrobenzoic acids; other temp.; |
Conditions | Yield |
---|---|
With Vilsmeier reagent; triethylamine In tetrahydrofuran at 20℃; for 16h; | 94% |
p-chlorophenoxymethyl chloride
2,4-dinitrobenzoic acid
2,4-Dinitro-benzoic acid 4-chloro-phenoxymethyl ester
Conditions | Yield |
---|---|
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane for 0.25h; Heating; | 93% |
Conditions | Yield |
---|---|
Stage #1: dicyclohexyl-carbodiimide; 2,4-dinitrobenzoic acid In dichloromethane at 20℃; for 0.5h; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; | 93% |
(5,5-difluoro-1,3,7,9-tetramethyl-5H-4λ4,5λ4-dipyrrolo[1,2-c:2′,1′-f ][1,3,2]diazaborinin-10-yl)methanol
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 16h; Inert atmosphere; | 91% |
Conditions | Yield |
---|---|
Stage #1: N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; 2,4-dinitrobenzoic acid In dichloromethane at 20℃; for 0.5h; Stage #2: With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; | 91% |
Conditions | Yield |
---|---|
With Bromotrichloromethane; trichloroisocyanuric acid; bromine at 10 - 120℃; for 18h; Photolysis; | 91% |
2-phenylethynylphenol
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)diiridium(I) dichloride In dichloromethane at 20℃; for 12h; regioselective reaction; | 91% |
tetrakis(acetato)dimolybdenum(II)
2,4-dinitrobenzoic acid
Mo2(O2CC6H3-2,4-(NO2)2)4
Conditions | Yield |
---|---|
In toluene byproducts: AcOH; N2-atmosphere; slight excess of substituted benzoic acid, stirring overnight; solvent removal (vac., gentle warming), repeated addn. of PhMe and evapn., dissoln. in THF, filtration, concn., cooling to -20°C overnight (pptn.); | 90% |
ammonium hydroxide
oxalyl dichloride
2,4-dinitrobenzoic acid
2,4-dinitrobenzamide
Conditions | Yield |
---|---|
89% |
2,2,2-Trinitroethyl hydrogen sulfate
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
at 50 - 55℃; for 1h; | 88% |
Conditions | Yield |
---|---|
In dichloromethane at 20℃; | 88% |
Conditions | Yield |
---|---|
With Vilsmeier reagent; triethylamine In tetrahydrofuran at 20℃; for 16h; | 87% |
(+)-(S)-4-phenylbutan-2-ol
2,4-dinitrobenzoic acid
C17H16N2O6
Conditions | Yield |
---|---|
With Vilsmeier reagent; triethylamine In tetrahydrofuran at 20℃; for 16h; | 86% |
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
Stage #1: 4-[5-(naphtho[2,1-b]furan-2-yl)-1,3,4-oxadiazol-2-yl]aniline With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; Inert atmosphere; Stage #2: 2,4-dinitrobenzoic acid In dichloromethane at 20℃; Inert atmosphere; | 86% |
2,4-dinitrobenzoic acid
allyltriisopropylsilane oxide
Conditions | Yield |
---|---|
In chloroform | 85% |
Conditions | Yield |
---|---|
With thionyl chloride In dichloromethane at 20℃; for 8.5h; | 83% |
With thionyl chloride In dichloromethane at 20℃; |
N,N-dimethyl-formamide
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
With trichlorophosphate at 120℃; for 1h; Sealed tube; | 83% |
With trichlorophosphate at 120℃; for 1h; | 83% |
2,4-dinitrobenzoic acid
Conditions | Yield |
---|---|
In dichloromethane at 0 - 20℃; | 83% |
glycerol
2,4-dinitrobenzoic acid
1,3-dichloro-2-propyl 2,4-dinitrobenzoate
Conditions | Yield |
---|---|
With chloro-trimethyl-silane at 80℃; for 48h; | 81% |
Conditions | Yield |
---|---|
In benzene at -20℃; for 6h; | 80.5% |
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