Bis(4-nitrophenyl) carbonate supplier

Name
Bis(4-nitrophenyl) carbonate
EINECS 225-775-4
CAS No. 5070-13-3
Article Data31
CAS DataBase
Density 1.501 g/cm³
Solubility
Melting Point 136-139 °C(lit.)
Formula C₁₃H₈N₂O₇
Boiling Point 475.9 °C at 760 mmHg
Molecular Weight 304.216
Flash Point 217.5 °C
Transport Information
Appearance white to pale yellow or beige powder
Safety 26-36
Risk Codes 36/38
Molecular Structure
Hazard Symbols Xi
Synonyms Carbonicacid, bis(p-nitrophenyl) ester (6CI,7CI,8CI);4,4'-Dinitrodiphenyl carbonate;Carbonic acid,bis(4-nitrophenyl) ester;Bis(p-nitrophenyl) carbonate;Di-4-nitrophenylcarbonate;Di-p-nitrophenyl carbonate;NSC 1730;p,p'-Dinitrodiphenylcarbonate;
PSA 127.17000
LogP 4.12720

Synthetic route

: 100-02-7
4-nitro-phenol

: 67-66-3
chloroform

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With oxygen; sodium hydrogencarbonate; triethylamine In water for 1h; Irradiation;	99%
With pyridine; oxygen at 30℃; for 6.5h; UV-irradiation;	39%
With oxygen; sodium hydroxide In water at 20℃; for 2h; Irradiation;	5%

: 102-09-0
bis(phenyl) carbonate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With mixed-acid; sulfuric acid; nitric acid In cyclohexane; ethyl acetate; nitrobenzene	94%
With nitric acid
With nitric acid In sulfuric acid; water

: 100-02-7
4-nitro-phenol

: 32315-10-9
bis(trichloromethyl) carbonate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran; dichloromethane at 0℃; for 0.583333h; Inert atmosphere;	91%
With triethylamine In tetrahydrofuran for 2h;	42%

: 93350-13-1
3-Hydroxy-3-phenyl-azocan-2-one

: 7693-46-1
4-Nitrophenyl chloroformate

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: 93350-09-5
1-aza-9,10-dioxo-8-oxa-7-phenylbicyclo<5.2.1>decane

Conditions

Conditions	Yield
In toluene for 24h; Heating;	A 0.20 g B 90%

...Expand

4-Hydroxymethyl-5-methyl-1,3-doxolene-2-one: 4-Hydroxymethyl-5-methyl-1,3-doxolene-2-one

: 7693-46-1
4-Nitrophenyl chloroformate

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: 173604-87-0
(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-nitrophenyl carbonate

Conditions

Conditions	Yield
With pyridine; hydrogenchloride In sodium hydroxide; chloroform	A 81% B n/a

...Expand

: 75-44-5
phosgene

: 824-78-2
4-nitrophenol sodium salt

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
In toluene at 60℃; for 3h;	78%
In benzene

: 7693-46-1
4-Nitrophenyl chloroformate

: 602-09-5
1,1'-bi-2-naphthol

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: 138537-48-1
3,5-Dioxa-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-one

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 5℃; for 1h;	A n/a B 78%

...Expand

: 100-02-7
4-nitro-phenol

: 4-nitrophenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With potassium tert-butylate In toluene at 20℃; for 0.25h; Green chemistry;	74%
With aluminum (III) chloride In toluene at 20℃; for 2h;	70%

: 75-44-5
phosgene

: 100-02-7
4-nitro-phenol

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With pyridine In toluene; benzene
With pyridine In toluene
(i) Py, (ii) /BRN= 1098367/, toluene; Multistep reaction;

: 7693-46-1
4-Nitrophenyl chloroformate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With ethyleneimine; triethylamine In diethyl ether
With pyridine In dichloromethane

: 100-02-7
4-nitro-phenol

: 503-38-8
trichloromethyl chloroformate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
In tetrahydrofuran for 0.166667h; Heating; Yield given;

: 102-09-0
bis(phenyl) carbonate

: 7697-37-2
nitric acid

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: 81420-42-0
mononitrophenyl carbonate

Conditions

Conditions	Yield
at -10 - -5℃;

...Expand

: 102-09-0
bis(phenyl) carbonate

: 7697-37-2
nitric acid

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: carbonic acid-(2-nitro-phenyl ester)-(4-nitro-phenyl ester)

C: 81420-42-0
mononitrophenyl carbonate

Conditions

Conditions	Yield
at -8℃; Product distribution;

...Expand

: 102-09-0
bis(phenyl) carbonate

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B <2-nitro-phenyl>-<4-nitro-phenyl>-carbonate , bis-<2-nitro-phenyl>-carbonate: <2-nitro-phenyl>-<4-nitro-phenyl>-carbonate , bis-<2-nitro-phenyl>-carbonate

Conditions

Conditions	Yield
With nitric acid at -8℃;

: 100-02-7
4-nitro-phenol

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 2: Et3N, aziridine / diethyl ether View Scheme

: 100-02-7
4-nitro-phenol

: 7693-46-1
4-Nitrophenyl chloroformate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With triethylamine In dichloromethane

: 2-[5-(2,5,8,11,14,17,20-heptaoxadocosan-22-yloxy)-2-nitrophenyl]ethanol

: 7693-46-1
4-Nitrophenyl chloroformate

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: C29H40N2O15

Conditions

Conditions	Yield
With triethylamine In dichloromethane for 24h; Darkness;

...Expand

: 5-(2,5,8,11,14,17,20-heptaoxadocosan-22-yloxy)-2-nitrotoluene

A: 5070-13-3
bis-(p-nitrophenyl) carbonate

B: C29H40N2O15

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: potassium tert-butylate / dimethyl sulfoxide / 0.5 h / 80 °C / Inert atmosphere 2: triethylamine / dichloromethane / 24 h / Darkness View Scheme

: 29526-99-6
1-methylcyclopropanol

: 7693-46-1
4-Nitrophenyl chloroformate

A: 1046817-22-4
1-methylcyclopropyl (4-nitrophenyl)carbonate

B: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With pyridine In dichloromethane-d2 at 20℃;

...Expand

: 4-nitrophenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate

: 5070-13-3
bis-(p-nitrophenyl) carbonate

Conditions

Conditions	Yield
With potassium carbonate In tetrahydrofuran for 18h; Reflux; Green chemistry;	239 mg

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1185503-80-3
C17H20F3N3*ClH

: 4-nitrophenyl [1-({1-[4-(trifluoromethyl)phenyl]-1H-pyrrol-3-yl}methyl)piperidin-4-yl]carbamate

Conditions

Conditions	Yield
In dichloromethane at 20℃; for 1.5h;	100%

: 110-89-4
piperidine

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1609109-07-0
(3R,4R,5R,7S)-5-{(1E,3E)-5-[(2S,3S,5R,6R)-5-{[(2Z,4S)-4-hydroxypent-2-enoyl]amino}-3,6-dimethyltetrahydro-2H-pyran-2-yl]-3-methylpenta-1,3-dien-1-yl}-7-[2-oxo-2-(propylamino)ethyl]-1,6-dioxaspiro[2.5]oct-4-yl acetate

: 1609106-61-7
(2S,3Z)-5-({(2R,3R,5S,6S)-6-[(2E,4E)-5-{(3R,4R,5R,7S)-4-(acetyloxy)-7-[2-oxo-2-(propylamino)ethyl]-1,6-dioxaspiro[2.5]oct-5-yl}-3-methylpenta-2,4-dien-1-yl]-2,5-dimethyltetrahydro-2H-pyran-3-yl}amino)-5-oxopent-3-en-2-yl piperidine-1-carboxylate

Conditions

Conditions	Yield
Stage #1: bis-(p-nitrophenyl) carbonate; (3R,4R,5R,7S)-5-{(1E,3E)-5-[(2S,3S,5R,6R)-5-{[(2Z,4S)-4-hydroxypent-2-enoyl]amino}-3,6-dimethyltetrahydro-2H-pyran-2-yl]-3-methylpenta-1,3-dien-1-yl}-7-[2-oxo-2-(propylamino)ethyl]-1,6-dioxaspiro[2.5]oct-4-yl acetate With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 16h; Stage #2: piperidine In dichloromethane at 20℃; for 0.25h;	100%

...Expand

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 74654-07-2
2-[2-(2-methoxyethoxy)ethoxy]ethylamine

: N,N′-bis(3,6,9-trioxadecyl)urea

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 3h; Inert atmosphere;	100%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C25H41N3O9

: C32H44N4O13

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0℃; for 3h;	100%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: N-(4-(O-ethyl-P-ethynyl-phosphonamidato-N-benzoyl))-L-valine-L-citrulline-4-aminobenzyl alcohol

: N-(4-(O-ethyl-P-ethynyl-phosphonamidato-N-benzoyl))-L-valine-L-citrulline-4-aminobenzyl-4-nitrophenyl carbonate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1h;	100%
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1h;

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: (2S,3R,4S,5S,6S)-2-(2-((S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanamido)propanamido)-5-(hydroxymethyl)phenoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: (2S,3R,4S,5S,6S)-2-(2-((S)-2-((S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanamido)propanamido)-5-((((4-nitrophenoxy)carbonyl)oxy)methyl)phenoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran Inert atmosphere;	100%

: 202350-68-3
(8S,10S)-6,8,11-trihydroxy-8-(2-hydroxyacetyl)-1-methoxy-10-(((1S,3R,4aS,9S,9aR,10aS)-9-methoxy-1-methyloctahydro-1H-pyrano[4’,3’:4,5]oxazolo[2,3-c][1,4]oxazin-3-yl)oxy)-7,8,9,10-tetrahydrotetracene-5,5,12-dione

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C39H38N2O17

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran; dichloromethane at 20℃; Darkness;	100%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1613321-01-9
N-(6-azidohexanoyl)-Val-Cit-4-aminobenzyl alcohol

: 1613321-02-0
N-(6-azidohexanoyl)-Val-Cit-4-aminobenzyl 4-nitrophenyl carbonate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 41h; Inert atmosphere;	99%
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: (3R,4S)-tert-butyl 3-(((S)-2-acetoxy-N-((R)-(1-benzyl-4-(2,5-difluorophenyl)-1H-imidazol-2-yl)(tetrahydro-2H-pyran-4-yl)methyl)propanamido)methyl)-4-hydroxypyrrolidine-1-carboxylate

: 110-58-7
1-pentanamine

: (3R,4S)-tert-butyl 3-(((S)-2-acetoxy-N-((R)-(1-benzyl-4-(2,5-difluorophenyl)-1H-imidazol-2-yl)(tetrahydro-2H-pyran-4-yl)methyl)propanamido)methyl)-4-((pentylcarbamoyl)oxy)pyrrolidine-1-carboxylate

Conditions

Conditions	Yield
Stage #1: bis-(p-nitrophenyl) carbonate; (3R,4S)-tert-butyl 3-(((S)-2-acetoxy-N-((R)-(1-benzyl-4-(2,5-difluorophenyl)-1H-imidazol-2-yl)(tetrahydro-2H-pyran-4-yl)methyl)propanamido)methyl)-4-hydroxypyrrolidine-1-carboxylate With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1h; Stage #2: n-Pentylamine In N,N-dimethyl-formamide at 20℃; for 1.5h;	99%

...Expand

: 56826-61-0
(2-methylpyridin-3-yl)methanol

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1198424-07-5
(2-methylpyridin-3-yl)methyl 4-nitrophenyl carbonate

Conditions

Conditions	Yield
With 4-methyl-morpholine In dichloromethane at 20℃; for 68h;	98%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 148579-57-1
(2S,3R,4S,5S,6S)-2-(4-(hydroxymethyl)phenoxy)-6-(methoxycarbonyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: (2S,3S,4S,5R,6S)-2-(methoxycarbonyl)-6-(4-((((4-nitrophenoxy)carbonyl)oxy)methyl)phenoxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran for 48h;	98%
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 18h; Inert atmosphere;	93%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: (9H-fluoren-9-yl)methyl ((80S,83S)-80-((4-(hydroxymethyl)phenyl)carbamoyl)-84-methyl-74,82-dioxo2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71-tetracosaoxa-75,81-diazapentaoctacontan-83-yl)carbamate

: (9H-fluoren-9-yl)methyl ((80S,83S)-84-methyl-80-((4-((((4-nitrophenoxy)carbonyl)oxy)methyl)phenyl)carbamoyl)-74,82-dioxo-2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,68,71-tetracosaoxa-75,81-diazapentaoctacontan-83-yl)carbamate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃;	98%

: C29H29N3O9S2

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C36H32N4O13S2

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl acetamide at 20℃; for 22h; Inert atmosphere;	97%

: 4070-48-8
L-Valine methyl ester

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 162537-10-2
N-<<(4-nitrophenyl)oxy>carbonyl>-L-valine methyl ester

Conditions

Conditions	Yield
With 4-methyl-morpholine In dichloromethane at 0℃; for 4h;	96%
With 4-methyl-morpholine In dichloromethane at 0℃; for 4h;	96%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 29968-78-3
2-(4-nitrophenyl)ethylamine monohydrochloride

: 1,3-bis(4-nitrophenylethyl)urea

Conditions

Conditions	Yield
With dmap; triethylamine In tetrahydrofuran at 20℃; Inert atmosphere;	96%
With triethylamine In N,N-dimethyl-formamide at 58 - 62℃; for 2h; Reagent/catalyst; Solvent;	86%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1343407-91-9
allyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1- oxopropan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate

: allyl ((S)-3-methyl-1-(((S)-1-((4-((((4-nitrophenoxy)carbonyl)-oxy)methyl)phenyl)amino)-1-oxopropan-2-yl)amino)-1-oxobutan-2-yl)carbamate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 1.5h;	96%
With N-ethyl-N,N-diisopropylamine at 20℃; for 13h;	87%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C8H10N2O3S2

: C15H13N3O7S2

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 15℃; for 3h;	95.8%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

A: 124-38-9
carbon dioxide

B: 101-63-3
bis(4-nitrophenyl)ether

Conditions

Conditions	Yield
at 200 - 270℃; Product distribution; Kinetics; Mechanism; investigation of effect of iniciators and substituents in reactions; Ea= 26kcal/mol;	A n/a B 95%
at 200 - 270℃;	A n/a B 95%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 108-91-8
cyclohexylamine

: 2387-23-7
1,3-Dicyclohexylurea

Conditions

Conditions	Yield
In dichloromethane for 4h; Ambient temperature;	95%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 1003-03-8
Cyclopentamine

: 58713-33-0
N,N'-Dicyclopentylurea

Conditions

Conditions	Yield
In dichloromethane for 4h; Ambient temperature;	95%

: 159857-80-4
6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)hexanamide

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 159857-81-5
N-[6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoyl]-L-valyl-N5-carbamoyl-N[4-({[(4-nitrophenoxy)carbonyl]oxy}methyl)phenyl]-L-ornithinamide

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 25℃;	95%
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 5h;	92%
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 18h; Inert atmosphere;	74%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C21H31N7O4

: C28H34N8O8

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 50℃; for 16h;	95%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: C17H27N3O3

: C24H30N4O7

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 0℃; for 3h;	95%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 111-27-3
hexan-1-ol

: 67036-15-1
p-nitrophenylcarbonate hexyl ester

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 25 - 30℃;	94.84%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: 89043-75-4
4-amino-3-deoxy-N10-formylpteroic acid

: 95485-01-1
p-nitrophenyl 4-amino-4-deoxy-N10-formylpteroate

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 25℃; for 18h;	94%

: 112-90-3, 1838-19-3, 22146-67-4
oleylamine

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: [N-(octadec-9-enyl)-carbamoyl]-p-nitrophenol

Conditions

Conditions	Yield
With dmap In tetrahydrofuran at 20℃; for 3h;	94%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: (3S,7S,10R,16S,E)-10-(3-chloro-4-methoxybenzyl)-16-((S)-1-((2R,3R)-3-(4-(hydroxymethyl)phenyl)oxiran-2-yl)ethyl)-6,6,7-trimethyl-3-neopentyl-1-oxa-4,8,11-triazacyclohexadec-13-ene-2,5,9,12-tetraone

: 4-((2R,3R)-3-((S)-1-((3S,7S,10R,16S,E)-10-(3-chloro-4-methoxybenzyl)-6,6,7-trimethyl-3-neopentyl-2,5,9,12-tetraoxo-1-oxa-4,8,11-triazacyclohexadec-13-en-16-yl)ethyl)oxiran-2-yl)benzyl (4-nitrophenyl) carbonate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 144h;	94%

: 5070-13-3
bis-(p-nitrophenyl) carbonate

: tert-butyl ((S)-1-(((S)-1-((4-(hydroxymethyl)phenyl)amino)-1-oxopropane-2-yl)amino)-3-methyl-1-oxobutan-2-yl)carbamate

: tert-butyl ((S)-3-methyl-1-(((S)-1-((4-((((4-nitrophenoxy)carbonyl)oxy)methyl)phenyl)amino)-1-oxopropan-2-yl)amino)-1-oxobutan-2-yl)carbamate

Conditions

Conditions	Yield
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃;	94%
With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h;	94%
With triethylamine In tetrahydrofuran at 20℃; for 2h;	77%

Bis(4-nitrophenyl) carbonate Chemical Properties

Molecule structure of Bis(4-nitrophenyl) carbonate (CAS NO.5070-13-3):

IUPAC Name: Bis(4-nitrophenyl) carbonate
Molecular Weight: 304.21182 g/mol
Molecular Formula: C₁₃H₈N₂O₇
Density: 1.501 g/cm³
Melting Point: 136-139 °C(lit.)
Boiling Point: 475.9 °C at 760 mmHg
Flash Point: 217.5 °C
Index of Refraction: 1.632
Molar Refractivity: 72.3 cm³
Molar Volume: 202.6 cm³
Surface Tension: 63.4 dyne/cm
Enthalpy of Vaporization: 73.95 kJ/mol
Vapour Pressure: 3.19E-09 mmHg at 25 °C
Sensitive: moisture sensitive
XLogP3-AA: 3.3
H-Bond Acceptor: 7
Rotatable Bond Count: 4
Exact Mass: 304.033151
MonoIsotopic Mass: 304.033151
Topological Polar Surface Area: 122
Heavy Atom Count: 22
Canonical SMILES: C1=CC(=CC=C1[N+](=O)[O-])OC(=O)OC2=CC=C(C=C2)[N+](=O)[O-]
InChI: InChI=1S/C13H8N2O7/c16-13(21-11-5-1-9(2-6-11)14(17)18)22-12-7-3-10(4-8-12)15(19)20/h1-8H
InChIKey: ACBQROXDOHKANW-UHFFFAOYSA-N
EINECS: 225-775-4
Product Categories of Bis(4-nitrophenyl) carbonate (CAS NO.5070-13-3): Industrial/Fine Chemicals

Bis(4-nitrophenyl) carbonate Safety Profile

Hazard Codes: Irritant Xi
Risk Statements: 36/38
R36/38:Irritating to eyes and skin.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
WGK Germany: 3
F: 10-21

Bis(4-nitrophenyl) carbonate Specification

Bis(4-nitrophenyl) carbonate (CAS NO.5070-13-3) is also named as 4,4'-Dinitrodiphenyl carbonate ; AI3-14990 ; Bis(p-nitrophenyl) carbonate ; NSC 1730 ; p,p'-Dinitrodiphenylcarbonate . Bis(4-nitrophenyl) carbonate (CAS NO.5070-13-3) is white to pale yellow or beige powder.

Product Name

Bis(4-nitrophenyl) carbonate

Synthetic route

Bis(4-nitrophenyl) carbonate Chemical Properties

Bis(4-nitrophenyl) carbonate Safety Profile

Bis(4-nitrophenyl) carbonate Specification

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