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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,
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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:Beijing or Guangzhou
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inquiry5-[BIS(METHYLSULFANYL)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:pharmaceutical intermediate Transportation:by air, by sea, by express
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inquiryfactory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
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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
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inquiryR & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
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inquiryHigh Quality Best Price Storage:Store in dry, dark and ventilated place Application:Chemical Synthesis Intermediate
1,3-Dioxane-4,6-dione,5-[bis(methylthio)methylene]-2,2-dimethyl- 100981-05-3 Storage:as prescribe by the manufacturer Package:pack as requested
Cas:100981-05-3
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inquirycarbon disulfide
cycl-isopropylidene malonate
methyl iodide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; cycl-isopropylidene malonate With triethylamine In dimethyl sulfoxide at 20℃; for 3h; Stage #2: methyl iodide In dimethyl sulfoxide | 81% |
Stage #1: carbon disulfide; cycl-isopropylidene malonate With triethylamine In dimethyl sulfoxide at 20℃; for 1h; Stage #2: methyl iodide In dimethyl sulfoxide at 20℃; Cooling; | 52% |
In dimethyl sulfoxide for 5h; Ambient temperature; | 50% |
methyl iodide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
Stage #1: cycl-isopropylidene malonate With carbon disulfide; triethylamine In dimethyl sulfoxide at 20℃; for 1h; Stage #2: methyl iodide In dimethyl sulfoxide at 0 - 20℃; for 15h; | 28.8% |
cycl-isopropylidene malonate
methyl iodide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
With carbon disulfide; triethylamine 1) DMSO, 1 h, rt, 2) 14 h; Yield given. Multistep reaction; | |
With carbon disulfide In N-methyl-acetamide; hexane; ethyl acetate; mineral oil; benzene |
methyl iodide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In dimethyl sulfoxide for 4h; Ambient temperature; Yield given; | |
In dimethyl sulfoxide at 0 - 20℃; for 4h; |
cycl-isopropylidene malonate
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dimethylsulfoxide / 1 h / Ambient temperature 2: dimethylsulfoxide / 4 h / Ambient temperature View Scheme |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethylamine
Conditions | Yield |
---|---|
In acetonitrile pH=7; | 100% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 99% |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 99% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
2-bromoaniline
5-[2-bromoanilino(methylthio)methylene]-2,2-dimethyl[1,3]dioxane-4,6-dione
Conditions | Yield |
---|---|
Stage #1: 5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione With 3-chloro-benzenecarboperoxoic acid In dichloromethane at 20℃; for 1h; Stage #2: 2-bromoaniline In 2,2,2-trifluoroethanol at 20℃; for 1.5h; Further stages.; | 98% |
In 2,2,2-trifluoroethanol for 22h; Heating / reflux; | 88% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
ethylenediamine
5-(imidazolidin-2-ylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 97% |
In dichloromethane for 3h; | 84% |
In methanol; chloroform |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 97% |
2-thiazolylamine
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
7-Methylthio-5-oxo-5H-thiazolo<3,2-a>pyrimidine-6-carboxylic acid
Conditions | Yield |
---|---|
In ethanol at 80 - 85℃; for 2.5h; | 96% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
N-methyl-ethane-1,2-diamine
2,2-dimethyl-5-(1-methyl-2-imidazolidinylidene)-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 2h; Heating; | 96% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
N-Methyl-1,3-propanediamine
isopropylidene (1-methyl-2-hexahydropyrimidinylidene)malonate
Conditions | Yield |
---|---|
In ethanol for 3h; Heating; | 96% |
2-(o-tolyloxy)aniline
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 9h; Heating; | 95.8% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Trimethylenediamine
isopropylidene (2-hexahydropyrimidinylidene)malonate
Conditions | Yield |
---|---|
In ethanol for 3h; Heating; | 95% |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 95% |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 95% |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 95% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Cysteamine
isopropylidene (2-thiazolidinylidene)malonate
Conditions | Yield |
---|---|
In ethanol for 8h; Heating; | 94% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
2,2-bis(aminomethyl)propane-1,3-diamine tetrahydrochloride
Conditions | Yield |
---|---|
With triethylamine In ethanol; water for 2.5h; Ambient temperature; | 93% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
4-fluoroaniline
5-[(4-fluorophenylamino)(methylthio)methylene]-2,2-dimethyl-4,6-dioxo-1,3-dioxane
Conditions | Yield |
---|---|
In chloroform at 60℃; for 0.5h; | 93% |
In ethanol for 2h; Reflux; | 78% |
methylmagnesium bromide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
methylamine hydrochloride
2,2-dimethyl-5-(1-methylamino-ethylidene)-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
Stage #1: methylmagnesium bromide; 5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione In tetrahydrofuran; diethyl ether at -4 - 20℃; for 1.16667h; Inert atmosphere; Stage #2: methylamine hydrochloride at 20℃; for 0.25h; Inert atmosphere; | 93% |
methylmagnesium bromide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
<15N>-methylamine hydrochloride
C9H13(15)NO4
Conditions | Yield |
---|---|
Stage #1: methylmagnesium bromide; 5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione In tetrahydrofuran; diethyl ether at -4 - 20℃; for 1.16667h; Inert atmosphere; Stage #2: <15N>-methylamine hydrochloride at 20℃; for 0.25h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 93% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
1-amino-2-propene
5-<(allylamino)(methylthio)methylene>-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 24h; Ambient temperature; | 91% |
methylmagnesium bromide
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
glycine ethyl ester hydrochloride
ethyl 2-(1-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ylidene)ethylamino)acetate
Conditions | Yield |
---|---|
Stage #1: methylmagnesium bromide; 5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione In tetrahydrofuran; diethyl ether at -4 - 20℃; for 1.16667h; Inert atmosphere; Stage #2: glycine ethyl ester hydrochloride at 20℃; for 0.25h; Inert atmosphere; | 91% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
With tris-(2-carboxyethyl)-phosphine hydrochloride In aq. phosphate buffer; acetonitrile pH=7.8; | 91% |
propylamine
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In acetonitrile at 20℃; for 24h; pH=7; | 91% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
isopropylamine
5-(Bis-isopropylamino-methylene)-2,2-dimethyl-[1,3]dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 48h; Ambient temperature; | 90% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
1,2-diamino-benzene
isopropylidene (2-benzimidazolinylidene)malonate
Conditions | Yield |
---|---|
In ethanol for 8h; Heating; | 90% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
4-Phenyl-3-thiosemicarbazide
Conditions | Yield |
---|---|
In water for 5h; Reflux; Green chemistry; | 90% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
2-amino-benzenethiol
5-(benzo[d]thiazol-2(3H)-ylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 12h; Heating; | 88% |
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
4-bromo-aniline
5-<4-Bromophenylamino(methylthio)methylene>-2,2-dimethyl-4,6-dioxo-1,3-dioxane
Conditions | Yield |
---|---|
In ethanol for 4h; Heating; | 88% |
In chloroform at 60℃; for 1h; | 88% |
In aq. phosphate buffer; acetonitrile pH=7; |
meta-fluoroaniline
5-[bis(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
5-[3-fluoroanilino(methylthio)methylene]-2,2-dimethyl-1,3-dioxane-4,6-dione
Conditions | Yield |
---|---|
In ethanol for 2h; Reflux; | 87% |
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