- Product Name(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione
- cas28092-62-8
- purity99%
Others
(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione
Reputable supplier selling (3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione 28092-62-8 with stock
- Molecular Formula:C19H18 N2 O3
- Molecular Weight:322.364
- Vapor Pressure:2.46E-13mmHg at 25°C
- Melting Point:117-119 °C(Solv: ethanol (64-17-5))
- Boiling Point:577.5°Cat760mmHg
- PKA:-1.33±0.20(Predicted)
- Flash Point:303.1°C
- PSA：49.85000
- Density:1.311g/cm3
- LogP:2.29420
(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione(Cas 28092-62-8) Usage
|
General Description |
(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione is a chemical compound with potential pharmaceutical properties. It belongs to the class of furo[3,4-d]imidazole-2,4-dione derivatives and has a unique structure with two benzyl groups attached to a tetrahydrofuran ring. This chemical compound has shown potential as an antifungal agent and has been studied for its inhibitory effects on the growth of certain fungi. Additionally, its unique molecular structure makes it an interesting candidate for further drug development research. The compound's potential pharmaceutical properties make it a subject of interest for researchers in the fields of medicinal chemistry and drug discovery. |
InChI:InChI=1/C19H18N2O3/c22-18-17-16(13-24-18)20(11-14-7-3-1-4-8-14)19(23)21(17)12-15-9-5-2-6-10-15/h1-10,16-17H,11-13H2/t16-,17-/m0/s1
28092-62-8 Relevant articles
Practical Synthesis of (+)-Biotin Key Intermediate by Calcium Borohydride Reduction and Temperature-Dependent Purity Upgrade during Crystallization
Seki, Masahiko,Takahashi, Yusuke
, p. 1950 - 1959 (2021/08/03)
An expedient synthesis of a key intermed...
METHOD FOR PRODUCING LACTONE COMPOUND
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Paragraph 0072-0073; 0075, (2021/05/28)
PROBLEM TO BE SOLVED: To provide a produ...
HYDRATE OF AMIDOALCOHOL COMPOUND, PRODUCTION METHOD THEREOF, AND PRODUCTION METHOD OF LACTONE COMPOUND
-
Paragraph 0024; 0029; 0089; 0114-0117, (2021/11/26)
PROBLEM TO BE SOLVED: To provide a hydra...
METHOD FOR PRODUCING AMIDE CARBOXYLIC ACID COMPOUND, AND METHOD FOR PRODUCING AMIDE ALCOHOL COMPOUND, AND METHOD FOR PRODUCING LACTONE COMPOUND
-
, (2021/06/11)
PROBLEM TO BE SOLVED: To provide a produ...
28092-62-8 Process route
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![(4S,5R)-5-(hydroxymethyl)-2-oxo-N-[(1R)-1-phenylethyl]-1,3-bis(phenylmethyl)-4-imidazolidinecarboxamide](/upload/2026/8/e9383e5544d44a4cbb002417ecf98e60_869c9d9d-2389-4adb-b4b5-3ec1e1bd9aef.png)
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(4S,5R)-5-(hydroxymethyl)-2-oxo-N-[(1R)-1-phenylethyl]-1,3-bis(phenylmethyl)-4-imidazolidinecarboxamide
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![(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione](/upload/2026/8/23e5f8621320405fad2ed4f9d79aac16_484c03af-171e-4611-8c8a-b6014123663a.png)
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28092-62-8
(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione
Conditions
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
1,4-dioxane; water;
for 5h;
Reflux;
|
100% |
|
With
hydrogenchloride;
In
water;
at 100 ℃;
for 0.25h;
|
98% |
|
With
hydrogenchloride;
In
water;
pH=1;
Reflux;
|
95.4% |
|
With
hydrogenchloride;
In
N,N-dimethyl acetamide;
at 100 ℃;
for 3h;
|
95% |
-
-
C34H31N2O6(1-)*C8H20N(1+)
-
-
28092-62-8
(3aS,6aR)-1,3-dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4-dione
Conditions
| Conditions | Yield |
|---|---|
|
With
lithium borohydride;
In
tetrahydrofuran; 5,5-dimethyl-1,3-cyclohexadiene; water;
at 35 - 60 ℃;
for 2h;
|
98.8% |
28092-62-8 Upstream products
-
28092-55-9
6ξ-acetoxy-1,3-dibenzyl-(3ar,6ac)-tetrahydro-furo[3,4-d]imidazole-2,4-dione
-
21035-81-4
(3aS)-1,3-dibenzyl-6ξ-hydroxy-(3ar,6ac)-tetrahydro-furo[3,4-d]imidazole-2,4-dione
-
95790-99-1
cis 1,3-Dibenzyl-4-hydroxy-2,3,3a,4,6,6a-hexahydro-furo<3,4-d>imidazol-2-one
-
26339-42-4
(4S,5R)-1,3-dibenzyl-1H-furo[3,4-d]imidazole-2,4,6-trione
28092-62-8 Downstream products
-
61253-80-3
(3aS)-1,3-dibenzyl-(3ar,6ac)-tetrahydro-selenolo[3,4-d]imidazole-2,4-dione
-
133709-67-8
cis 4-Butyl-1,3-dibenzyl-4-hydroxy-2,3,3a,4,6,6a-hexahydrofuro<3,4-d>imidazol-2-one
-
95790-99-1
cis 1,3-Dibenzyl-4-hydroxy-2,3,3a,4,6,6a-hexahydro-furo<3,4-d>imidazol-2-one
-
133709-72-5
cis 1,3-Dibenzyl-4-(hex-5'-enyl)-4-hydroxy-2,3,3a,4,6,6a-hexahydrofuro<3,4-d>imidazol-2-one
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