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5-Benzyl-2,4-imidazolinedione GMP Manufacturer Global Trade 3530-82-3 with Fast Delivery
- Molecular Formula: C10H10N2O2
- Molecular Weight: 190.202
- Appearance/Colour: Crystalline solid
- Melting Point: 188-189 °C
- Refractive Index: 1.57
- PKA: 8.88±0.10(Predicted)
- PSA： 58.20000
- Density: 1.251 g/cm3
- LogP: 1.09470
5-Benzyl-2,4-imidazolinedione(Cas 3530-82-3) Usage
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Synthesis Reference(s) |
The Journal of Organic Chemistry, 39, p. 2644, 1974 DOI: 10.1021/jo00931a049 |
InChI:InChI=1/C10H10N2O2/c13-9-8(11-10(14)12-9)6-7-4-2-1-3-5-7/h1-5,8H,6H2,(H2,11,12,13,14)/t8-/m1/s1
3530-82-3 Relevant articles
Pd-Catalysed oxidative carbonylation of α-amino amides to hydantoins under mild conditions
Botla, Vinayak,Carfagna, Carla,Della Ca, Nicola,Gabriele, Bartolo,Maestri, Giovanni,Mancuso, Raffaella,Montanari, Luca,Motti, Elena,Voronov, Aleksandr
supporting information, p. 294 - 297 (2022/01/06)
The first example of palladium-catalysed...
Facile One-Pot Synthesis of Substituted Hydantoins from Carbamates
Tanwar, Dinesh Kumar,Ratan, Anjali,Gill, Manjinder Singh
supporting information, p. 2285 - 2290 (2017/10/06)
A novel and simple approach for the prep...
Identification of a New Zinc Binding Chemotype by Fragment Screening
Chrysanthopoulos, Panagiotis K.,Mujumdar, Prashant,Woods, Lucy A.,Dolezal, Olan,Ren, Bin,Peat, Thomas S.,Poulsen, Sally-Ann
, p. 7333 - 7349 (2017/09/22)
The discovery of a new zinc binding chem...
Continuous Synthesis of Hydantoins: Intensifying the Bucherer-Bergs Reaction
Monteiro, Julia L.,Pieber, Bartholom?us,Corrêa, Arlene G.,Kappe, C. Oliver
supporting information, p. 83 - 87 (2015/12/26)
A continuous Bucherer-Bergs hydantoin sy...
3530-82-3 Process route
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potassium cyanide
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506-87-6,6721-33-1,10361-29-2
ammonium carbonate
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122-78-1
phenylacetaldehyde
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3530-82-3
5-benzyl-hydantoin
Conditions
| Conditions | Yield |
|---|---|
|
In
methanol; water;
at 50 - 60 ℃;
for 3h;
|
81%
|
|
In
water; ethyl acetate;
at 120 ℃;
for 0.533333h;
under 15001.5 Torr;
Flow reactor;
|
72%
|
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622-46-8
carbamic acid phenyl ester
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5619-07-8
methyl 2-amino-3-phenylpropanoate hydrochloride
-
-
3530-82-3
5-benzyl-hydantoin
Conditions
| Conditions | Yield |
|---|---|
|
carbamic acid phenyl ester; methyl 2-amino-3-phenylpropanoate hydrochloride;
With
triethylamine;
In
acetonitrile;
for 10h;
Reflux;
With
sodium hydroxide;
In
acetonitrile;
for 8h;
Reflux;
|
73%
|
3530-82-3 Upstream products
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590-28-3
potassium cyanate
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150-30-1
Phenylalanine
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54896-72-9
(R)-3-phenyl-2-ureido-propionic acid
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949-45-1
(S)-3-phenyl-2-ureido-propionic acid
3530-82-3 Downstream products
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21109-49-9
5-(α-bromo-benzylidene)-imidazolidine-2,4-dione
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113806-19-2
N-3-(2'-hydroxypropyl)-5-benzylhydantoin
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113806-19-2
N-3-(2'-hydroxypropyl)-5-benzylhydantoin
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133384-55-1
5-benzyl-3-(1-methoxycarbonyl-2-phenylethyl)hydantoin
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