DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:2682-49-7
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryItems Standard Result Assay (Ursolic acid) 98%min 98.22% ----------------------------------------------------------------
Cas:2682-49-7
Min.Order:1 Gram
FOB Price: $100.0 / 500.0
Type:Trading Company
inquiryUnique advantages for 1,3-THIAZOLIDIN-2-ONE Cas 2682-49-7 Guaranteed the purity High quality & competitive price Quality control Fast feedback Prompt shipment Appearance:White Powder Package:1kg/foil bag, 25kg/drum or as you
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Min.Order:1 Gram
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Type:Manufacturers
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Cas:2682-49-7
Min.Order:1 Metric Ton
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Type:Manufacturers
inquiryProduct Name: 1,3-THIAZOLIDIN-2-ONE Synonyms: 2-Thiazolidinone;Thiazolidine-2-one;1,3-THIAZOLIDIN-2-ONE;THIAZOLIDIN-2-ONE;1,3-Tetrahydro-2-thiazolone;1,3-THIAZOLIDINE-2-ONE;1,3-Thiazolan-2-one;2-Oxothiazoli
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Min.Order:1 Kilogram
Negotiable
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Min.Order:1 Kilogram
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Type:Trading Company
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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Min.Order:1 Kilogram
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inquiry1. Characteristics Item Specification CAS 2682-49-7 Appearance White or white like powder 2. Application: It is an important non-o-benzene solid plasticizer and has g
Our 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
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Cas:2682-49-7
Min.Order:10 Gram
Negotiable
Type:Other
inquiryAppearance:White powder Storage:Room temperature Package:25kg/drum Application:Used as an acid bright copper plating additive Transportation:Express/Sea/Air Port:Any port in china
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Min.Order:25 Kilogram
Negotiable
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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
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inquiryCAS:2682-49-7 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, steroids, p
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Min.Order:1 Gram
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Cas:2682-49-7
Min.Order:500 Kilogram
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Type:Lab/Research institutions
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
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Min.Order:1 Gram
Negotiable
Type:Trading Company
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
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Min.Order:0 Metric Ton
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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
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inquiryProduct name: Thiozolidone CAS No.: 2682-49-7 Molecule Formula:C3H5NOS Molecule Weight:103.14 Purity: 98.0% Package: 25kg/drum Description:White powder Manufacture Standards:Enterprise Standard TESTING ITEMS
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Conditions | Yield |
---|---|
With selenium; oxygen; acetonitrile | 98% |
Stage #1: carbon monoxide; Cysteamine With potassium carbonate; sulfur In N,N-dimethyl-formamide at 20℃; under 760 Torr; for 4h; Stage #2: With oxygen In N,N-dimethyl-formamide at 20℃; under 760 Torr; for 2h; | 87% |
Conditions | Yield |
---|---|
at 180℃; for 3h; Temperature; Time; Concentration; | 85% |
Conditions | Yield |
---|---|
With potassium hydroxide In methanol at 20℃; for 1h; | 80% |
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 1h; Sealed tube; | 78% |
2-mercaptoethylamine hydrochloride
1,1'-carbonyldiimidazole
thiazolidine-2-one
Conditions | Yield |
---|---|
Stage #1: 2-mercaptoethylamine hydrochloride; 1,1'-carbonyldiimidazole With 18-crown-6 ether; potassium carbonate In acetonitrile for 18h; Heating; Stage #2: With water In acetonitrile for 4h; Heating; Further stages.; | 68% |
In ethanol for 15h; Ambient temperature; | 63% |
Stage #1: 2-mercaptoethylamine hydrochloride; 1,1'-carbonyldiimidazole With potassium carbonate; 18-crown-6 ether In acetonitrile at 80℃; for 19h; Heating / reflux; Stage #2: With sodium carbonate In water for 1h; Heating / reflux; | 42% |
thiazolidine-2-thione
thiazolidine-2-one
Conditions | Yield |
---|---|
With sodium; 2-bromoethanol In ethanol for 4h; Inert atmosphere; Reflux; | 56% |
With sodium ethanolate; 2-bromoethanol In ethanol at 60℃; for 4h; |
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol for 4h; Inert atmosphere; Reflux; | 56% |
(2-mercapto-ethyl)-carbamic acid ethyl ester
thiazolidine-2-one
Conditions | Yield |
---|---|
With hydrotalcite; magnesium aluminum In toluene for 5h; Heating; | 50% |
thiazolidine-2-one
Conditions | Yield |
---|---|
With sodium hydroxide |
S-(2-aminoethyl)-S’-benzyldithiocarbonate hydrochloride
thiazolidine-2-one
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With butan-1-ol |
Conditions | Yield |
---|---|
With toluene |
S-(2-aminoethyl)-S’-benzyldithiocarbonate hydrochloride
thiazolidine-2-one
Conditions | Yield |
---|---|
With selenium; CO; oxygen In tetrahydrofuran |
Conditions | Yield |
---|---|
With N-ethyl-N,N-diisopropylamine In diethyl ether; benzene |
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile for 2.5h; Reflux; | 100% |
Conditions | Yield |
---|---|
In acetonitrile byproducts: H2; Electrochem. Process; electrolyse of a soln. of the ligand in acetonitrile (NH4BF4) with a Nianode at room temp. under N2; filtered, washed with acetonitrile, dried in vac.; elem. anal.; | 99% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 99% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 98% |
Conditions | Yield |
---|---|
In acetonitrile byproducts: H2; Electrochem. Process; electrolyse of a soln. of the ligands in acetonitrile (NH4BF4) with a Ni anode at room temp. under N2; filtered, washed with acetonitrile, dried in vac.; elem. anal.; | 96% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 95% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 95% |
Conditions | Yield |
---|---|
With sodium methansulfinate; tetrabutylammomium bromide; potassium carbonate In tetrahydrofuran at 50℃; for 5h; Green chemistry; regioselective reaction; | 93% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 93% |
Conditions | Yield |
---|---|
With C29H30F6NOPS In 1,2-dichloro-ethane at 20℃; stereoselective reaction; | 85% |
thiazolidine-2-one
5-chloro-1-methyl-4-nitroimidazole
3-(3-Methyl-5-nitro-3H-imidazol-4-yl)-thiazolidin-2-one
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 15 - 100℃; for 2.25h; | 83% |
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In toluene at 130℃; for 6h; Inert atmosphere; Molecular sieve; | 78% |
thiazolidine-2-one
Conditions | Yield |
---|---|
With 3,3-dimethyl-2-nitroso-2,3-dihydrobenzo[d]isothiazole 1,1-dioxide; trifluoroacetic acid In acetonitrile at 20℃; Sealed tube; | 78% |
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In acetonitrile for 16h; Heating; | 72% |
With potassium carbonate; 18-crown-6 ether In acetonitrile for 17h; Heating / reflux; | 55% |
thiazolidine-2-one
ibuprofen
Conditions | Yield |
---|---|
Stage #1: ibuprofen With dmap; dicyclohexyl-carbodiimide In dichloromethane at 20℃; for 0.333333h; Stage #2: thiazolidine-2-one In dichloromethane at 20℃; for 4h; | 70% |
thiazolidine-2-one
Conditions | Yield |
---|---|
With lithium oxide Microwave irradiation; | 70% |
thiazolidine-2-one
(S)-5-(tert-butoxy)-4-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)-5-oxopentanoic acid
Conditions | Yield |
---|---|
Stage #1: (S)-5-(tert-butoxy)-4-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)-5-oxopentanoic acid With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: thiazolidine-2-one In N,N-dimethyl-formamide for 16h; | 65% |
With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 16h; | 42% |
thiazolidine-2-one
1-bromo-2-(bromomethyl)-4,5-dimethoxybenzene
C12H14BrNO3S
Conditions | Yield |
---|---|
Stage #1: thiazolidine-2-one With sodium hydride In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Stage #2: 1-bromo-2-(bromomethyl)-4,5-dimethoxybenzene In tetrahydrofuran Reflux; Inert atmosphere; | 63% |
thiazolidine-2-one
2,3-dimethoxy-6-bromobenzyl bromide
C12H14BrNO3S
Conditions | Yield |
---|---|
Stage #1: thiazolidine-2-one With sodium hydride In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Stage #2: 6-bromo-2,3-dimethoxybenzyl bromide In tetrahydrofuran Reflux; Inert atmosphere; | 61% |
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride; acetic acid In acetonitrile at 60℃; for 3h; Electrochemical reaction; Inert atmosphere; | 59% |
thiazolidine-2-one
2,2′-(naphthalene-1,4-diylbis(((4-methoxyphenyl)sulfonyl)azanediyl))diacetic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide | 58% |
Stage #1: 2,2′-(naphthalene-1,4-diylbis(((4-methoxyphenyl)sulfonyl)azanediyl))diacetic acid With dmap; dicyclohexyl-carbodiimide In N,N-dimethyl-formamide at 20℃; for 0.5h; Stage #2: thiazolidine-2-one In N,N-dimethyl-formamide | 0.368 g |
Conditions | Yield |
---|---|
With phosphorus(V) oxybromide at 110℃; for 3h; | 57% |
Conditions | Yield |
---|---|
Stage #1: thiazolidine-2-one With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0℃; for 0.166667h; Stage #2: 2-(tert-butoxycarbonylamino)ethyl bromide In N,N-dimethyl-formamide at 20℃; for 2h; | 51% |
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