p-benzoquinone
9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
In 2-ethoxy-ethanol at 125℃; for 4h; Inert atmosphere; | 93% |
In toluene at 110℃; for 3.5h; Temperature; Inert atmosphere; | 92% |
In toluene at 120℃; for 5h; Inert atmosphere; | 91.2% |
2,5-dihydroxy-1-iodobenzene
9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); sodium acetate In 1,4-dioxane at 100℃; for 12h; Inert atmosphere; | 65% |
2-bromobenzene-1,4-diol
9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With tetrakis(triphenylphosphine) palladium(0); sodium acetate In 1,4-dioxane at 100℃; for 24h; Inert atmosphere; | 25% |
Diisopropyl chlorophosphate
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 93% |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
dibutyl chlorophosphate
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 89.2% |
diethyl chlorophosphate
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 82.6% |
dipropyl chlorophosphate
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 80.5% |
Dimethyl chlorophosphate
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 78% |
di(sec-butyl) phosphoryl chloride
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 20℃; for 8h; Reflux; | 76.2% |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
cyanogen chloride
C20H11N2O4P
Conditions | Yield |
---|---|
With triethylamine In acetone at -9 - -6℃; for 2.75h; | 75% |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
2-(6-oxido-6H-dibenzo[c,e][1,2]oxaphosphinine-6-yl)cyclohexa-2,5-diene-1,4-dione
Conditions | Yield |
---|---|
With manganese(IV) oxide In acetone at 20℃; for 1h; | 68.8% |
4-Fluoronitrobenzene
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide at 160℃; for 12h; Inert atmosphere; | 67% |
With cesium fluoride In N,N-dimethyl acetamide at 160℃; for 10h; | 55.55% |
4-Vinylbenzyl chloride
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
Stage #1: 10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide With sodium hydroxide In toluene at 70℃; for 0.5h; Stage #2: 4-Vinylbenzyl chloride With tetrabutylammomium bromide In toluene at 70℃; for 10h; | 65% |
Stage #1: 10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide With sodium hydroxide In toluene at 70℃; for 0.5h; Stage #2: 4-Vinylbenzyl chloride With tetrabutylammomium bromide In toluene for 10h; | 65% |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran | 58% |
4'-octyloxy(1,1'-biphenyl)-4-carboxylic acid
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran for 6h; | 28% |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
4-{4-[2-(2-methoxyethoxy)ethoxy]phenyl} benzoic acid
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran | 27% |
epichlorohydrin
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With sodium methylate Etherification; | |
With N-benzyl-N,N,N-triethylammonium chloride at 95℃; for 4h; Reagent/catalyst; Temperature; Inert atmosphere; |
4'-n-hexyloxybiphenyl-4-carboxylic acid
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
formaldehyd
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
3,4-difluoroaniline
C34H23F4N2O4P
Conditions | Yield |
---|---|
at 90℃; |
formaldehyd
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
Heating; |
4-Fluoronitrobenzene
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
B
1,4'-bis(4-nitrophenoxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl acetamide at 160℃; for 12h; Inert atmosphere; |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
6-(2-(diphenylphosphoryl)-3,6-dihydroxyphenyl)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: manganese(IV) oxide / acetone / 1 h / 20 °C 2: toluene / 3 h / Inert atmosphere; Reflux View Scheme |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
6-(2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)-3,6-dihydroxyphenyl)-6H-dibenzo[c,e][1,2]oxaphosphinine 6-oxide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: manganese(IV) oxide / acetone / 1 h / 20 °C 2: toluene / 3 h / Inert atmosphere; Reflux View Scheme |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
6-(4-hydroxy-3-(6-oxido-6H-dibenzo[c,e][1,2]-oxaphosphinine-6-yl)phenoxy)-6H-dibenzo[c,e][1,2]-oxaphosphinine 6-oxide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: manganese(IV) oxide / acetone / 1 h / 20 °C 2: toluene / 3 h / Inert atmosphere; Reflux 3: triethylamine / toluene / 120 h / Reflux View Scheme |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: manganese(IV) oxide / acetone / 1 h / 20 °C 2: toluene / 3 h / Inert atmosphere; Reflux View Scheme |
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: manganese(IV) oxide / acetone / 1 h / 20 °C 2: toluene / 3 h / Inert atmosphere; Reflux View Scheme |
teroxirone
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
at 150℃; for 5h; |
Allyl ether
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Conditions | Yield |
---|---|
With magnesium sulfate; 3-chloro-benzenecarboperoxoic acid In chloroform at 25℃; for 8h; Inert atmosphere; |
α-Naphthol Orange
1,4-bis[4-(carbonochloridoyl)phenyl] benzene-1,4-dicarboxylate
10‑(2,5‑dihydroxyphenyl)‑10H-9‑oxa‑10‑phosphaphenanthrene‑10‑oxide
Empirical Formula: C18H13O4P
Molecular Weight: 324.2672g/mol
Structure of 1,4-Benzenediol,2-(6-oxido-6H-dibenz[c,e][1,2]oxaphosphorin-6-yl)- (CAS NO.99208-50-1):
Index of Refraction: 1.722
Molar Refractivity: 85.657 cm3
Molar Volume: 216.443 cm3
Polarizability: 33.957×10-24cm3
Surface Tension: 76.6 dyne/cm
Density: 1.498 g/cm3
Flash Point: 312.364 °C
Enthalpy of Vaporization: 91.669 kJ/mol
Meliting Point: 245-255 °C
Boiling Point: 592.882 °C at 760 mmHg
Vapour Pressure: 0 mmHg at 25°C
Product Categories: Industrial/Fine Chemicals
Systematic Name: 2-(6-Oxido-6H-dibenzo[c,e][1,2]oxaphosphinin-6-yl)benzene-1,4-diol
SMILES: Oc1cc(c(O)cc1)P3(=O)Oc4ccccc4c2ccccc23
InChI: InChI=1/C18H13O4P/c19-12-9-10-15(20)18(11-12)23(21)17-8-4-2-6-14(17)13-5-1-3-7-16(13)22-23/h1-11,19-20H
InChIKey: KMRIWYPVRWEWRG-UHFFFAOYAE
1,4-Benzenediol,2-(6-oxido-6H-dibenz[c,e][1,2]oxaphosphorin-6-yl)- , its cas register number is 99208-50-1. It also can be called 2-(6-Oxido-6H-dibenzo[c,e][1,2]oxaphosphinin-6-yl)benzene-1,4-diol .
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