Conditions | Yield |
---|---|
With sulfuric acid; bromine; tin(IV) chloride at 30 - 80℃; for 13h; Reagent/catalyst; Temperature; | 95.1% |
With sulfuric acid; bromine; iodine | |
With sulfuric acid; bromine at 60℃; anschliessend Erhitzen auf 200grad; | |
With sulfuric acid; bromine at 60℃; anschliessend Erhitzen auf 200grad; |
tetrabromobenzene-1,2-dicarboxylic acid
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
durch Sublimation; |
phthalic anhydride
sulfuric acid
bromine
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
at 60℃; anschl. Erhitzen auf 200grad; | |
at 60℃; anschl. Erhitzen auf 200grad; |
Conditions | Yield |
---|---|
With iron(III) chloride; sulfuric acid; bromine; iodine at 50 - 150℃; for 3h; |
piperidine
Tetrabromophthalic anhydride
4,5,6,7-tetrabromo-3-hydroxy-3-piperidinophthalide
Conditions | Yield |
---|---|
In ethyl acetate for 1h; Heating; | 99% |
Tetrabromophthalic anhydride
4-(2-aminoethyl)benzenesulfonamide
4-(2-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)ethyl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 1.5h; Inert atmosphere; | 99% |
With acetic acid for 12h; Reflux; |
Tetrabromophthalic anhydride
methyl N-[5(6)-(4-aminophenylsulfanyl)benzimidazol-2-yl]carbamate
Conditions | Yield |
---|---|
With sodium acetate; acetic acid at 40 - 45℃; for 3h; | 98% |
D-tert-leucine
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
With triethylamine In toluene Reflux; | 97% |
Tetrabromophthalic anhydride
tetrabromobenzene-1,2-dicarboxylic acid
Conditions | Yield |
---|---|
Stage #1: Tetrabromophthalic anhydride With potassium hydroxide In water for 0.5h; Inert atmosphere; Reflux; Stage #2: With hydrogenchloride In water at 20℃; Inert atmosphere; | 96% |
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl acetamide at 55℃; for 3.5h; Temperature; Concentration; Reagent/catalyst; Solvent; | 95.6% |
Tetrabromophthalic anhydride
3,4-dicyanoaniline
Conditions | Yield |
---|---|
In acetic acid for 2h; Reflux; | 95.5% |
Tetrabromophthalic anhydride
3,4,5,6-tetrabromophthalimide
Conditions | Yield |
---|---|
With iron(III) chloride; guanidine hydrochloride; triethylamine at 60℃; for 0.0833333h; | 95% |
With formamide In neat (no solvent) for 0.333333h; Reagent/catalyst; Milling; Heating; Green chemistry; | 94% |
With choline chloride; urea at 140℃; for 1h; Green chemistry; | 92% |
With potassium cyanate In N,N-dimethyl-formamide for 0.05h; microwave irradiation; | 89% |
Tetrabromophthalic anhydride
4-(hydrazinecarbonyl)benzene-1-sulfonamide
Conditions | Yield |
---|---|
With sodium acetate; acetic acid for 12h; Reflux; | 95% |
Tetrabromophthalic anhydride
3,4,5-Trimethoxyaniline
4,5,6,7-tetrabromo-2-(3,4,5-trimethoxyphenyl)isoindoline-1,3-dione
Conditions | Yield |
---|---|
With acetic acid for 12h; Reflux; | 94% |
Tetrabromophthalic anhydride
2,3-diamino-1,4-naphthoquinone
1,2,3,4-tetrabromonaphtho[2',3':4,5]imidazo[2,1-a]isoindole-6,11,13-trione
Conditions | Yield |
---|---|
With acetic acid In water at 20℃; Reflux; | 94% |
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 1.5h; Inert atmosphere; | 94% |
1-((1R,2R)-2-aminocyclohexyl)-3-(3,5-bis(trifluoromethyl)phenyl)thiourea
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 8h; Inert atmosphere; | 94% |
With dmap In tetrahydrofuran at 20℃; for 2h; | |
With triethylamine In tetrahydrofuran Inert atmosphere; Schlenk technique; |
Conditions | Yield |
---|---|
With titanium tetrachloride In 1,2,3-trichlorobenzene at 100 - 195℃; for 3h; | 93.9% |
Conditions | Yield |
---|---|
With sodium acetate; acetic acid for 12h; Reflux; | 93% |
piperidine
Tetrabromophthalic anhydride
piperidinium 3,4,5,6-tetrabromo-2-piperidinocarbonylbenzoate
Conditions | Yield |
---|---|
In benzene | 92% |
Conditions | Yield |
---|---|
In toluene for 5h; Heating; | 92% |
In toluene Condensation; Heating; | |
In toluene for 3h; Condensation; Heating; Dean-Stark conditions; |
Tetrabromophthalic anhydride
C15H14BrN
4,5,6,7-tetrabromo-2-(4-bromo-phenyl)-isoindoline-1,3-dione
Conditions | Yield |
---|---|
In ethanol for 1h; Reflux; | 92% |
Tetrabromophthalic anhydride
m-aminobenzenesulfonamide
3-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 2h; Inert atmosphere; | 92% |
Tetrabromophthalic anhydride
4-amino-2-chlorobenzenesulfonamide
3-chloro-4-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 12h; Inert atmosphere; | 92% |
Conditions | Yield |
---|---|
In diethyl ether | 91.09% |
Tetrabromophthalic anhydride
sulfanilamide
4-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid for 20h; Reflux; | 91% |
With acetic acid at 130℃; for 12h; Inert atmosphere; | 75% |
3,4-dihydro-6-hydroxy-2,5,7,8-tetramethyl-2H-benzopyran-2-carbohydrazide
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
With acetic acid for 2h; Reflux; | 91% |
Tetrabromophthalic anhydride
4-amino-2-fluorobenzenesulfonamide
3-fluoro-4-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 12h; Inert atmosphere; | 90% |
Tetrabromophthalic anhydride
4-amino-2-bromobenzenesulfonamide
3-bromo-4-(4,5,6,7-tetrabromo-1,3-dioxoisoindolin-2-yl)benzenesulfonamide
Conditions | Yield |
---|---|
With acetic acid at 130℃; for 12h; Inert atmosphere; | 90% |
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 8h; Inert atmosphere; | 90% |
Tetrabromophthalic anhydride
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran for 8h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With niobium pentachloride In methanesulfonic acid at 95 - 100℃; for 1.66667h; Friedel-Crafts Acylation; Inert atmosphere; | 90% |
With Zn0.95*Ti0.05O In neat (no solvent) at 160℃; for 4h; Green chemistry; | 66% |
Tetrabromophthalic anhydride
2,6-diisopropylbenzenamine
Conditions | Yield |
---|---|
With acetic acid at 140℃; for 12h; | 90% |
1. | eye-rbt 100 mg MLD | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0523271 . | ||
2. | orl-rat LD50:>10 g/kg | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0539755 . | ||
3. | ihl-rat LC :>10,920 mg/m3/4H | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0522251 . | ||
4. | skn-rbt LD50:>10 g/kg | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0522251 . | ||
5. | skn-gpg LD50:>1 g/kg | NTIS** National Technical Information Service. (Springfield, VA 22161) (Formerly U.S. Clearinghouse for Scientific and Technical Information) OTS0521611 . |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View