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Cas:68-35-9
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryItems Standard Result Appearance White yellowish-white crystalline power or crystals conform Assay (drid basis)
Cas:68-35-9
Min.Order:1 Gram
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Type:Manufacturers
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Min.Order:1 Gram
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Type:Manufacturers
inquiryUnique advantages for BP Sulfadiazine Cas 68-35-9 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:Powder Storage:0-6°C Package:1kg/foil bag, 25kg/drum or as you require
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Min.Order:25 Kilogram
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Type:Trading Company
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inquiryCompetive price Top quality Competitive price Product Information: Product name: Sulfadiazine Other name: N1-(Pyrimidin-2-yl)sulfanilamide CAS#: 68-35-9 W M:
Cas:68-35-9
Min.Order:1 Kilogram
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inquiryhigh quality Appearance:white powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea Port:shanghai
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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Min.Order:1 Gram
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Type:Manufacturers
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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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Cas:68-35-9
Min.Order:25 Kilogram
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Type:Other
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Min.Order:1 Metric Ton
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Type:Lab/Research institutions
inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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Type:Trading Company
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inquirysulfadiazine discount 68-35-9 98%MIN factory EINECS number 200-685-8 Molecular formula C10H10N4O2S MDL number MFCD00006065 Molecular weight 250.28 MOL file 68-35-9.mol Physicochemical properties Appearance traits White or almost whit
Cas:68-35-9
Min.Order:1 Gram
FOB Price: $15.0
Type:Lab/Research institutions
inquiry(1) High quality (2) Competitive price (3) First-class service and product (4) Environment friendly (5) Great performance (6) Easy application Appearance:White powder Storage:sealed and stored in cool places. Package:25kg drum Application
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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Cas:68-35-9
Min.Order:10 Gram
FOB Price: $3.5
Type:Trading Company
inquiryWuhan hanweishi Pharmchem Co., Ltd(Hanways chempharm) is a specialized company concentrating on the R&D, production, marketing and technical service of APIs and pharmaceutical intermediates. The leading products range are APIs, Hormones, Peptides
Cas:68-35-9
Min.Order:100 Kilogram
FOB Price: $1.0 / 5.0
Type:Trading Company
inquirySynonyms: PYRIMAL;N1-(PYRIMIDIN-2-YL)SULFANILAMIDE;N1-2-PYRIMIDINYLSULFANILAMIDE;SULFADIAZIN;SULFADIAZINE;STERAZINE;SULPHADIAZINE;TIMTEC-BB SBB007604 CAS: 68-35-9 MF: C10H10N4O2S MW: 250.28 EINECS: 200-685-8 Product Categories: Antibiotics for
Cas:68-35-9
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryAbout Product Details Items Specifications Test Results Appearance White to white crystalline powde
Cas:68-35-9
Min.Order:100 Kilogram
FOB Price: $1.0 / 2.0
Type:Lab/Research institutions
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Min.Order:1 Kilogram
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Type:Trading Company
inquirySulfadiazine CAS:68-35-9 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 intermediates,
Cas:68-35-9
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
Stage #1: 2-aminopyrimidine; p-acetylaminobenzenesulfonyl chloride With calcium carbonate In toluene at 20 - 65℃; Stage #2: With water; sodium hydroxide In toluene at 100 - 115℃; Stage #3: With acetic acid pH=5 - 5.5; Reagent/catalyst; | 98.5% |
Stage #1: 2-aminopyrimidine; p-acetylaminobenzenesulfonyl chloride With pyridine In tetrahydrofuran at 20℃; for 6h; Inert atmosphere; Stage #2: With sodium hydroxide for 2h; Inert atmosphere; Reflux; | 65% |
Stage #1: 2-aminopyrimidine; p-acetylaminobenzenesulfonyl chloride With pyridine In tetrahydrofuran at 20℃; for 6h; Stage #2: With sodium hydroxide for 2h; Reflux; |
N-benzylidene-sulfanilic acid pyrimidin-2-ylamide
sulfadiazine
Conditions | Yield |
---|---|
With water In acetone at 20℃; for 0.666667h; Irradiation; | 98% |
4-amino-N-(diaminomethylene) benzenesulfonamide
3-ethoxyacrolein
sulfadiazine
Conditions | Yield |
---|---|
In ethanol at 100℃; for 4h; Green chemistry; | 91% |
3-butoxyacrolein
4-amino-N-(diaminomethylene) benzenesulfonamide
sulfadiazine
Conditions | Yield |
---|---|
In butan-1-ol at 100℃; for 4h; Green chemistry; | 90.8% |
Malondialdehyde
1-amino-4-({[amino(imino)methyl]amino}sulfonyl)benzene
sulfadiazine
Conditions | Yield |
---|---|
With sodium methylate In methanol at 65℃; for 2h; Temperature; | 89% |
3-methoxyacrolein
4-amino-N-(diaminomethylene) benzenesulfonamide
sulfadiazine
Conditions | Yield |
---|---|
In methanol at 100℃; for 4h; Temperature; Green chemistry; | 87% |
2-aminopyrimidine
3-(4-acetylamino-benzenesulfonyl)-2-benzenesulfonylimino-2,3-dihydro-thiazole
sulfadiazine
Conditions | Yield |
---|---|
und anschliessenden Erhitzen mit wss. NaOH; |
Conditions | Yield |
---|---|
und anschliessenden Erhitzen mit wss. NaOH; |
Conditions | Yield |
---|---|
With potassium carbonate |
Conditions | Yield |
---|---|
With potassium carbonate |
4-nitro-N-pyrimidin-2-ylbenzenesulfonamide
sulfadiazine
Conditions | Yield |
---|---|
With hydrogenchloride; iron | |
With palladium 10% on activated carbon In tetrahydrofuran; methanol; ethyl acetate at 50℃; under 37503.8 Torr; | |
With hydrogenchloride; iron |
Conditions | Yield |
---|---|
With calcium hydroxide | |
With hydrogenchloride | |
With sodium hydroxide | |
With sodium hydroxide In methanol; 1,2-dimethoxyethane at 120℃; for 16h; | |
With sodium hydroxide |
sulfadiazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: aq. NaOH solution View Scheme | |
Multi-step reaction with 2 steps 1: pyridine / acetonitrile / 3.08 h / 60 °C 2: sodium hydroxide / methanol; 1,2-dimethoxyethane / 16 h / 120 °C View Scheme |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: amin-salt; dild. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: amin-salt; dild. acids; |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
Multi-step reaction with 3 steps 1: mineral acids 3: mineral acids View Scheme |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
Multi-step reaction with 3 steps 1: mineral acids 3: mineral acids View Scheme |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: Ag-salt; dild. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
Multi-step reaction with 3 steps 1: mineral acids 3: mineral acids View Scheme |
sulfadiazine
Conditions | Yield |
---|---|
With mineral acids byproducts: Ag-salt; concd. acids; | |
With mineral acids byproducts: Ag-salt; concd. acids; | |
Multi-step reaction with 3 steps 1: mineral acids 3: mineral acids View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: pyridine / 100 °C 2: palladium 10% on activated carbon / methanol; ethyl acetate; tetrahydrofuran / 50 °C / 37503.8 Torr View Scheme |
silver sulfadiazine
sulfadiazine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 2: mineral acids View Scheme | |
Multi-step reaction with 2 steps 2: mineral acids View Scheme | |
Multi-step reaction with 2 steps 2: mineral acids View Scheme |
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone for 3h; Darkness; | 97% |
Conditions | Yield |
---|---|
With acetic acid In ethanol for 4h; Reflux; | 96.3% |
In ethanol for 2.5h; Schiff Reaction; Reflux; | 62% |
sulfadiazine
water
cobalt(II) diacetate tetrahydrate
[cobalt(II)(sulfadiazine(-1H))2(H2O)2]
Conditions | Yield |
---|---|
In water byproducts: Na acetate; Na salt of ligand dissolved in H2O; Co salt in H2O added dropwise with stirring at 40°C for 1 h; filtered; ppt. washed with H2O, MeOH and Et2O successively; dried under vac.; elem. anal.; | 96% |
Conditions | Yield |
---|---|
In water byproducts: NaCl; Na salt of ligand dissolved in H2O; Co salt in H2O added dropwise with stirring at 40°C for 1 h; filtered; ppt. washed with H2O, MeOH and Et2O successively; dried under vac.; elem. anal.; | 96% |
sulfadiazine
ethyl acetoacetate
3-oxo-N-{4-[(pyrimidin-2-ylamino)sulphonyl]phenyl}butanamide
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide for 3h; | 95% |
at 140℃; for 0.25h; | 75% |
methanol
sulfadiazine
cobalt(II) diacetate tetrahydrate
[cobalt(II)(sulfadiazine(-1H))2(methanol)2]
Conditions | Yield |
---|---|
In methanol byproducts: Na acetate; Na salt of ligand dissolved in MeOH; Co salt in MeOH added dropwise withstirring at 40°C for 1 h; filtered; ppt. washed with H2O, MeOH and Et2O successively; dried under vac.; elem. anal.; | 95% |
Conditions | Yield |
---|---|
In methanol byproducts: NaCl; Na salt of ligand dissolved in MeOH; Co salt in MeOH added dropwise withstirring at 40°C for 1 h; filtered; ppt. washed with H2O, MeOH and Et2O successively; dried under vac.; elem. anal.; | 95% |
1-oxa-4-aza-spiro[4.4]nonane
formaldehyd
sulfadiazine
C18H23N5O3S
Conditions | Yield |
---|---|
In ethanol; water for 4h; Reflux; | 95% |
sulfadiazine
1-n-butyl-3-methylimidazolim bromide
C8H15N2(1+)*C10H9N4O2S(1-)
Conditions | Yield |
---|---|
Stage #1: 1-n-butyl-3-methylimidazolim bromide With Merck ion exchange resin III In water Stage #2: sulfadiazine In water at 20℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With acetic acid at 120℃; for 0.166667h; | 94% |
sulfadiazine
Conditions | Yield |
---|---|
Stage #1: sulfadiazine With sulfuric acid; sodium nitrite In water at 0 - 5℃; for 0.25h; Stage #2: (E)-N-[(2-chloroquinolin-3-yl)methylene]-4-phenylthiazol-2-amine With sodium hydroxide In ethanol; water for 1h; pH=5 - 6; Cooling with ice; | 93% |
sulfadiazine
n-hexadecanoyl chloride
N-palmitoyl-sulfanilic acid pyrimidin-2-ylamide
Conditions | Yield |
---|---|
With pyridine for 48h; Ambient temperature; | 92% |
Conditions | Yield |
---|---|
Stage #1: sulfadiazine With hydrogenchloride; sodium nitrite In ethanol at 0 - 5℃; Stage #2: 2-Mercaptobenzothiazole With sodium hydroxide In ethanol at 5 - 20℃; for 6h; | 92% |
N-(2-chloropyrimidin-4-yl)-2,3-dimethyl-2H-indazol-6-amine
sulfadiazine
4-((4-((2,3-dimethyl-2H-indazol-6-yl)amino)pyrimidin-2-yl)amino)-N-(pyrimidin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With hydrogenchloride In water; isopropyl alcohol at 85℃; | 92% |
Conditions | Yield |
---|---|
Stage #1: 1-octyl-3-methyl-imidazolium bromide With Merck ion exchange resin III In water Stage #2: sulfadiazine In water at 20℃; for 2h; | 92% |
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Reflux; | 91% |
sulfadiazine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 10 - 50℃; for 3h; | 91% |
sulfadiazine
Conditions | Yield |
---|---|
With water In acetone react. at 75°C for 1 h; ppt.; elem. anal.; | 90% |
With water In methanol react. at 75°C for 1 h; ppt.; elem. anal.; | 90% |
sulfadiazine
Conditions | Yield |
---|---|
With water In methanol react. at 60°C; pptn. after several hours; filtration (glass filter); washing of the ppt. with MeOH, H2O, EtOH and ether; elem. anal.; | 90% |
Conditions | Yield |
---|---|
In methanol; water mixt. Cu(2+) salt and ligand was dissolved in MeOH, concd. ammonia soln.was added dropwise and stirred for 10 min; slow evapn. at room temp.; elem. anal.; | 90% |
Conditions | Yield |
---|---|
In methanol; water mixt. Cu(2+) salt and ligand was dissolved in MeOH, concd. ammonia soln.was added dropwise and stirred for 10 min; slow evapn. at room temp.; elem. anal.; | 90% |
4-fluorocinnamic acid
sulfadiazine
Conditions | Yield |
---|---|
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane Reflux; | 90% |
sulfadiazine
acetylacetone
4-{2-[2,4-dioxopentan-3-ylidene]hydrazinyl}-N-(pyrimidin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
Stage #1: sulfadiazine With hydrogenchloride; sodium nitrite In water; acetic acid at 0 - 5℃; Stage #2: acetylacetone With sodium acetate In ethanol; water; acetic acid at 0 - 20℃; for 2h; | 90% |
sulfadiazine
3-methyl-1-tosyl-1H-pyrazol-5(4H)-one
Conditions | Yield |
---|---|
With hydrogenchloride; sodium acetate; sodium nitrite In ethanol; water at 0 - 5℃; for 1h; | 90% |
Conditions | Yield |
---|---|
Stage #1: sulfadiazine With hydrogenchloride; sodium nitrite In water at 0 - 70℃; for 0.0833333h; Stage #2: 1H-benzimidazol-2-acetonitrile With sodium acetate In ethanol at 0 - 5℃; | 90% |
Conditions | Yield |
---|---|
Stage #1: 2-aminopyrimidine With hydrogenchloride; sodium nitrite In water at 0 - 5℃; Stage #2: sulfadiazine With sodium hydroxide In water at 0 - 5℃; pH=7; | 89.5% |
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