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Cas:1086-00-6
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inquiryLower 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
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
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Ansciep 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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We are committed to providing our customers with the best products and services at the most competitive prices.Appearance:white to light yellow crystal powder Storage:Room temperature with sealed well Package:according to the clients requirement Appl
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Pyrene,1-(chloromethyl)- cas 1086-00-6Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 1-CHLOROMETHYLPYRENE, CAS:1086-00-6 with the most competitive price and the best qual
Pyrene,1-(chloromethyl)-Appearance:Off white to slight yellow solid Storage:Store in dry and cool condition Package:25kg or according to cutomer's demand Application:Chemical research/Pharmaceutical intermediates Transportation:By Sea,by Air,By couri
Debyesci is here who supplied several kinds of chemical products to global pharmaceutical, drug discovery, agrochemical and biotechnology industries for four yearsOur key scientific leadership team has gained experience in top research and developmen
1-pyrenemethanol
1-chloromethylpyrene
Conditions | Yield |
---|---|
With thionyl chloride In toluene for 12h; Heating; | 100% |
With hydrogenchloride; sodium sulfate In toluene for 5h; | 97% |
With thionyl chloride In benzene Ambient temperature; | 96% |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaBH4 / CHCl3; ethanol 2: SOCl2 / pyridine; diisopropyl ether View Scheme | |
Multi-step reaction with 2 steps 1: 86 percent / NaBH4 / ethanol / 6 h / Ambient temperature 2: 96 percent / SOCl2 / benzene / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 1: NaBH4 2: 85 percent / PCl3 View Scheme |
(2-nitrophenyl)(pyren-1-ylmethyl)selane
A
1-pyrenemethanol
B
1-chloromethylpyrene
Conditions | Yield |
---|---|
With sodium hypochlorite In chloroform-d1; water |
(2-nitrophenyl)(pyren-1-ylmethyl)selane
1-chloromethylpyrene
Conditions | Yield |
---|---|
With sodium hypochlorite; tetrabutyl-ammonium chloride In chloroform-d1; water |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium tetrahydroborate / methanol / Inert atmosphere 1.2: 20 h / 20 °C / Inert atmosphere 2.1: sodium hypochlorite / chloroform-d1; water View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: sodium tetrahydroborate / methanol / Inert atmosphere 1.2: 20 h / 20 °C / Inert atmosphere 2.1: sodium hypochlorite; tetrabutyl-ammonium chloride / chloroform-d1; water View Scheme |
1-chloromethylpyrene
phosphoric acid dibenzyl ester
dibenzyl pyren-1-ylmethyl phosphate
Conditions | Yield |
---|---|
With silver(l) oxide In acetonitrile at 20℃; for 6h; | 99% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 99% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 99% |
1-chloromethylpyrene
methyl 3-hydroxy-5-hexadecoxy benzoate
methyl 3-hexadecoxy-5-pyrenemethoxyl benzoate
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In tetrahydrofuran; acetonitrile for 20h; Heating; | 98% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 98% |
1-chloromethylpyrene
(S)-2-Benzyloxycarbonylamino-pentanedioic acid 5-methyl ester
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 98% |
(4-hydroxyphenyl)methanol
1-chloromethylpyrene
[4-(Pyren-1-ylmethoxy)-phenyl]-methanol
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In tetrahydrofuran; acetonitrile for 24h; Heating; | 96% |
1-chloromethylpyrene
Conditions | Yield |
---|---|
Stage #1: ethyl 3,4,6-tri-O-allyl-1-thio-β-D-glucopyranoside With sodium hydride In N,N-dimethyl-formamide Stage #2: 1-chloromethylpyrene In N,N-dimethyl-formamide at 20℃; for 3h; | 96% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 93% |
Diethyl phosphate
1-chloromethylpyrene
diethyl pyren-1-ylmethyl phosphate
Conditions | Yield |
---|---|
With silver(l) oxide In acetonitrile for 3.5h; Product distribution; Ambient temperature; various reaction conditions; | 92% |
With silver(l) oxide In acetonitrile for 3.5h; Ambient temperature; | 92% |
With silver(l) oxide In acetonitrile for 3.5h; Ambient temperature; | 92% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; | 91% |
rac-3-sulfanylpropane-1,2-diol
1-chloromethylpyrene
3-(pyren-1-ylmethylthio)-propane-1,2-diol
Conditions | Yield |
---|---|
With triethylamine In toluene at 20℃; for 20h; | 90% |
1-chloromethylpyrene
methylamine
N,N-dimethyl-1-(pyren-1-yl)methanamine
Conditions | Yield |
---|---|
In dichloromethane for 24h; Reflux; | 85% |
1-chloromethylpyrene
4,4'-dimethoxytrityl chloride
CYTIDINE
4-N-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(1-pyrenylmethyl)cytidine
Conditions | Yield |
---|---|
Multistep reaction.; | 84% |
1-chloromethylpyrene
(benzyloxy)carbamic acid 1,1-dimethylethyl ester
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 80 - 90℃; for 3h; | 79% |
Conditions | Yield |
---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 20℃; for 0.75h; Inert atmosphere; | 78% |
1-chloromethylpyrene
triethyl phosphite
Diethyl <(1-pyrenyl)methyl>phosphonate
Conditions | Yield |
---|---|
for 4h; Heating; | 76% |
for 12h; Reflux; | 75% |
1-chloromethylpyrene
1,2-O-isopropylidene-D-glycerol
(S)-1-O-(pyren-1-ylmethyl)glycerol
Conditions | Yield |
---|---|
Stage #1: 1-chloromethylpyrene; 1,2-O-isopropylidene-D-glycerol With potassium hydroxide In toluene Stage #2: With water; acetic acid at 20℃; Further stages.; | 75% |
Conditions | Yield |
---|---|
With silver(l) oxide In acetonitrile at 20℃; for 47h; | 72% |
1-chloromethylpyrene
tert-butyl N-(benzyloxy)carbamate
O-benzyl-N-(tert-butoxycarbonyl)-N-(1-pyrenyl)hydroxylamine
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 80 - 90℃; for 3h; | 71% |
Conditions | Yield |
---|---|
With potassium iodide In acetonitrile at 20℃; for 48h; | 71% |
2-[(S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethanol
1-chloromethylpyrene
(S)-2,2-dimethyl-4-[2-(pyren-1-ylmethoxy)ethyl]-[1,3]dioxolane
Conditions | Yield |
---|---|
With potassium hydroxide In toluene for 24h; Heating; | 67% |
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide at 20℃; for 48h; | 65% |
1-chloromethylpyrene
2'-deoxy-2'-mercaptouridine
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 20℃; for 17h; Inert atmosphere; | 64% |
4,4'-dimethyl-2,2'-bipyridines
1-chloromethylpyrene
4-methyl-4’-[2-(1-pyrenyl)ethyl]-2,2’-bipyridyl
Conditions | Yield |
---|---|
Stage #1: 4,4'-dimethyl-2,2'-bipyridines With lithium diisopropyl amide In tetrahydrofuran at -10℃; for 0.833333h; Stage #2: 1-chloromethylpyrene In tetrahydrofuran at 20℃; for 20h; Further stages.; | 63% |
Conditions | Yield |
---|---|
Stage #1: C34H24O4 With sodium hydride In N,N-dimethyl-formamide for 1h; Inert atmosphere; Stage #2: 1-chloromethylpyrene In N,N-dimethyl-formamide at 20℃; for 12h; Inert atmosphere; | 58% |
1-chloromethylpyrene
(3R,4S)-4-[(1S)-1,2-dihydroxyethyl]-3-hydroxypyrrolidine
N-(pyren-1-ylmethyl)-(3R,4S)-4-[(1S)-1,2-dihydroxyethyl]pyrrolidin-3-ol
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 20℃; | 57% |
Conditions | Yield |
---|---|
With triethylamine In benzene Heating; | 57% |
tert-butyl (3-(1H-imidazol-1-yl)propyl)carbamate
1-chloromethylpyrene
C28H30N3O2(1+)*Cl(1-)
Conditions | Yield |
---|---|
With sodium iodide In tetrahydrofuran at 100℃; for 2h; Microwave irradiation; | 52% |
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