3-nitro-benzoyl glycine
benzyl isothiocyanate
A
N-[2-[[[3-[[[(phenylmethyl)amino]carbonyl]amino]phenyl]carbonyl]amino]acetyl]-β-alanine
B
benzylurea
Conditions | Yield |
---|---|
With aniline; palladium In diethyl ether; ethanol; acetonitrile | A n/a B 99% |
Conditions | Yield |
---|---|
With merrifield anchored iron(II)-anthra catalyst In 1,4-dioxane at 100℃; for 8h; Temperature; Time; | 96% |
With choline chloride; tin(ll) chloride at 130℃; for 8h; Green chemistry; | 89% |
With cholin chloride ZnCl2; iron oxide at 130℃; for 6h; Green chemistry; | 86% |
Conditions | Yield |
---|---|
With ammonia In 1,4-dioxane | 95% |
Conditions | Yield |
---|---|
With N,N,N',N'-tetramethylguanidinium acetate In water at 60℃; for 0.5h; | 91% |
With hydrogenchloride In water at 20℃; for 6h; Solvent; Inert atmosphere; | 89% |
With hydrogenchloride In water at 80℃; for 1h; Microwave irradiation; | 88% |
Conditions | Yield |
---|---|
With zirconocene dichloride In n-heptane at 100℃; for 24h; Inert atmosphere; Sealed tube; | 87% |
Conditions | Yield |
---|---|
With [bis(acetoxy)iodo]benzene; ammonia In methanol at 0 - 20℃; for 2h; Hofmann Rearrangement; Inert atmosphere; | 86% |
Conditions | Yield |
---|---|
With Acetaldehyde oxime; cerium(IV) oxide In ethanol for 2h; Reflux; Inert atmosphere; | 84% |
With [OsCl2(η6-p-cymene)(PMe2OH)]; water at 40℃; for 0.5h; Reagent/catalyst; Inert atmosphere; Sealed tube; | 74% |
With hydrogenchloride | |
With hydrogenchloride In ethanol; water for 3h; Reflux; Inert atmosphere; | 0.1093 g |
Conditions | Yield |
---|---|
In water at 70℃; | 79% |
In water at 70℃; for 1h; | 79% |
Conditions | Yield |
---|---|
71% | |
Multi-step reaction with 4 steps 2: aqueous ethanol; hydrazine 3: aqueous hydrochloric acid; sodium nitrite 4: water View Scheme | |
Multi-step reaction with 2 steps 1: diethyl ether 2: hydrochloric acid View Scheme |
benzylurea
Conditions | Yield |
---|---|
With potassium hydroxide In methanol for 4h; | 70% |
Conditions | Yield |
---|---|
In water-d2; [D3]acetonitrile at 60℃; for 168h; pH=8.53; Acidic conditions; | A n/a B 70% |
Conditions | Yield |
---|---|
With ammonium acetate; water; triphenylphosphine In 1,4-dioxane at 20℃; for 24h; | 67% |
Conditions | Yield |
---|---|
for 48h; Ambient temperature; | 63% |
N-acetylphenylacetamidoxime
benzylurea
Conditions | Yield |
---|---|
With potassium hydroxide In methanol for 18h; Ambient temperature; | 59% |
chloromethyl N-benzyl carbamate
benzylurea
Conditions | Yield |
---|---|
With ammonium hydroxide In hexane for 2h; Ambient temperature; | 22% |
Conditions | Yield |
---|---|
With hydrogenchloride; dimethyl sulfoxide In water at 30℃; for 96h; | A 20% B 20% |
Conditions | Yield |
---|---|
With hydrogenchloride; 1,1-Dichloroacetone; dimethyl sulfoxide In water at 30℃; | A 20% B 20% |
Conditions | Yield |
---|---|
With sulfuric acid In toluene at 115℃; for 8h; | A 17% B 14% |
With sulfuric acid In toluene at 115℃; for 8h; | A 0.45 g B 0.2 g |
Conditions | Yield |
---|---|
at 190℃; |
benzyl-aminooxalyl azide
benzylurea
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With ethanol; ammonia anschliessendes Hydrieren an Raney-Nickel bei 130-180grad unter Druck; |
Conditions | Yield |
---|---|
With water | |
With ammonia; sodium |
N'-hydroxy-2-phenylethanimidamide
benzenesulfonyl chloride
A
benzylurea
B
N-benzenesulfonyloxy-2-phenyl-acetamidine
Conditions | Yield |
---|---|
With chloroform; sodium carbonate |
Conditions | Yield |
---|---|
With ethanol; ammonia |
Conditions | Yield |
---|---|
nachfolgende Hydrolyse mit wss. KOH; |
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
In water Heating; | |
With hydrogenchloride In water for 3h; Heating; |
Conditions | Yield |
---|---|
In ethanol Heating; |
Conditions | Yield |
---|---|
With dihydrogen peroxide In ethanol |
benzylurea
benzylammonium
Conditions | Yield |
---|---|
With water; dinitrogen tetraoxide for 0.5h; Ambient temperature; | 100% |
benzylurea
Glyoxilic acid
2,2-dihydroxyacetic acid
A
1-benzyl-5-hydroxy-hydantoin
Conditions | Yield |
---|---|
Stage #1: benzylurea; Glyoxilic acid; 2,2-dihydroxyacetic acid With acetic acid In water at 100℃; for 1h; Stage #2: With acetic acid In dichloromethane; water at 25℃; for 12h; | A 97.2% B 2.8% |
benzylurea
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In toluene at 110℃; Inert atmosphere; | 97% |
2-bromobenzoic acid methyl ester
benzylurea
3-benzylquinazoline-2,4-dione
Conditions | Yield |
---|---|
With tris(dibenzylideneacetone)dipalladium (0); caesium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene In 1,4-dioxane at 100℃; for 48h; | 95% |
benzylurea
Conditions | Yield |
---|---|
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In toluene at 110℃; Inert atmosphere; | 94% |
3-Iodotoluene
benzylurea
9-methyl-9H-fluorene-9-carbonyl chloride
N-(benzylcarbamoyl)-3-methylbenzamide
Conditions | Yield |
---|---|
With potassium phosphate; tri-tert-butyl phosphine; N-ethyl-N,N-diisopropylamine; bis(dibenzylideneacetone)-palladium(0); catacxium A In 1,4-dioxane at 90℃; for 18h; Inert atmosphere; | 93% |
benzylurea
methyl 3,3,3-trifluoro-2-(3-methyl-5-oxo-1-phenyl-4,5-dihydro-1Н-pyrazol-4-ylidene)propanoate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 2h; | 93% |
1,9-dimethyl-3H-pyrano<3,4-b>indol-3-one
benzylurea
4-benzyl-5,6-dimethyl-4,6-dihydro[1,3]diazepino[5,6-b]indol-3(2H)-one
Conditions | Yield |
---|---|
In bromobenzene for 3.5h; Reflux; | 92% |
Conditions | Yield |
---|---|
With polyphosphate ester In tetrahydrofuran for 15h; Heating; | 91% |
With tin(II) chloride dihdyrate In acetonitrile at 70 - 75℃; Biginelli Pyrimidone Synthesis; Sonication; | 71% |
With tin(II) chloride dihdyrate In acetonitrile Biginelli Pyrimidone Synthesis; Sonication; Heating; | |
With tin(II) chloride dihdyrate In acetonitrile at 70 - 75℃; Biginelli Pyrimidone Synthesis; Sonication; |
C14H13NO2
benzylurea
4-benzyl-5-ethyl-6-methyl-4,6-dihydro[1,3]diazepino[5,6-b]indol-3(2H)-one
Conditions | Yield |
---|---|
In bromobenzene for 8h; Reflux; | 91% |
benzylurea
1-ethyl-pyrano<3,4-b>indol-3-one
4-benzyl-5-ethyl-4,6-dihydro[1,3]diazepino[5,6-b]indol-3(2H)-one
Conditions | Yield |
---|---|
In bromobenzene for 4.5h; Reflux; | 91% |
methyl 3,3,3-trifluoro-2-(4-fluorobenzoylimino)propionate
benzylurea
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 90℃; for 3h; | 90% |
methyl 2-[(pyrimidin-2-yl)imino]-3,3,3-trifluoropropanoate
benzylurea
methyl 2-(3-benzylcarbamoylamino)-2-(pyrimidin-2-ylamino)-3,3,3-trifluoropropionate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 2h; | 90% |
Conditions | Yield |
---|---|
With acetic anhydride; N,N,N',N'-tetramethylguanidinium acetate at 60℃; for 1h; Neat (no solvent); | 89% |
Stage #1: cyanoacetic acid With acetic anhydride In dichloromethane for 0.0833333h; Stage #2: benzylurea In dichloromethane at 20℃; for 24h; Further stages.; | 44% |
With acetic anhydride for 2h; Heating; | |
With acetic anhydride at 80℃; for 2h; Inert atmosphere; | |
With acetic anhydride at 60℃; |
Conditions | Yield |
---|---|
With triethylsilane; trifluoroacetic acid In toluene at 22℃; for 18h; | 89% |
benzylurea
1-methylpyrano[3,4-b]indol-3(9H)-one
4-benzyl-5-methyl-4,6-dihydro[1,3]diazepino[5,6-b]indol-3(2H)-one
Conditions | Yield |
---|---|
In bromobenzene for 3h; Reflux; | 89% |
Conditions | Yield |
---|---|
With caesium carbonate at 120℃; for 1h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Microwave irradiation; Green chemistry; | 89% |
Conditions | Yield |
---|---|
In tetrahydrofuran at 0 - 20℃; | 88% |
In diethyl ether for 2h; Heating; | 21% |
In tetrahydrofuran for 3h; Ambient temperature; |
α,α-dihydroxyperfluoropropionic acid
benzylurea
3-benzyl-5-hydroxy-5-trifluoromethylimidazolidine-2,4-dione
Conditions | Yield |
---|---|
With sulfuric acid In 1,4-dioxane for 1.5h; Heating; | 88% |
sulfuric acid In 1,4-dioxane for 1.5h; Heating; | 88% |
methyl 3,3,3-trifluoro-2-[(1,3-benzothiazol-2-yl)imino]propanoate
benzylurea
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 90℃; for 3h; | 88% |
benzylurea
methyl 2-benzoylimino-3,3,3-trifluoropropionate
5-benzoylamino-3-benzyl-5-trifluoromethylimidazolidine-2,4-dione
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 90℃; | 88% |
Conditions | Yield |
---|---|
With sodium ethanolate In ethanol Reflux; | 88% |
With ethanol; sodium for 72h; Reflux; Inert atmosphere; | 86% |
With sodium ethanolate Reflux; | 72% |
benzylurea
methyl 2-(diethoxyphosphoryl)imino-3,3,3-trifluoropropionate
Conditions | Yield |
---|---|
In benzene for 1h; | 88% |
Conditions | Yield |
---|---|
With cholin chloride ZnCl2; iron oxide at 130℃; for 6h; Green chemistry; | 88% |
benzylurea
Methyl 2-Acetylimino-3,3,3-trifluoropropionate
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 90℃; for 3h; | 87% |
IUPAC Name: Benzylurea
Synonyms: (Phenylmethyl)urea ; 1-Benzylurea ; Urea, N-(phenylmethyl)- ; 1-Benzylharnstoff
Product Categories: BA - BHOrganic Building Blocks;Alphabetic;B;Carbonyl Compounds;Ureas
Molecular Structure of Benzylurea (CAS NO.538-32-9) :
Molecular Formula of Benzylurea (CAS NO.538-32-9) : C8H10N2O
Molecular Weight of Benzylurea (CAS NO.538-32-9) : 150.18
CAS NO: 538-32-9
EINECS : 208-689-1
Mol File: 538-32-9.mol
Merck : 14,1147
BRN : 2208083
Index of Refraction: 1.565
Surface Tension: 47.3 dyne/cm
Density: 1.138 g/cm3
Flash Point: 124.9 °C
Enthalpy of Vaporization: 52.18 kJ/mol
Boiling Point: 282.9 °C at 760 mmHg
Vapour Pressure: 0.00326 mmHg at 25°C
Melting point : 149-151 ºC
Appearance:white to off-white powder
Benzylurea (CAS NO.538-32-9) is used as intermediate organic synthesis.
1. | orl-rat LD50:4410 mg/kg | GISAAA Gigiena i Sanitariya. 44 (3)(1979),68. | ||
2. | orl-mus LD50:570 mg/kg | JMCMAR Journal of Medicinal Chemistry. 11 (1968),814. | ||
3. | orl-rat LD50:2700 mg/kg | GISAAA Gigiena i Sanitariya. 44 (3)(1979),68. |
Moderately toxic by ingestion. When heated to decomposition it emits toxic fumes of NOx.
Safety Statements 24/25-22
S24/25:Avoid contact with skin and eyes.
S22:Do not breathe dust.
WGK Germany 2
RTECS YS1780000
1.General Information: As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear.
2.Extinguishing Media: Use water spray, dry chemical, carbon dioxide, or chemical foam .
3.Handling: Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes. Avoid ingestion and inhalation.
4.Storage: Store in a cool, dry place. Store in a tightly closed container.
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