Reputable factory supply .trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione 26340-00-1 in bulk at low price

Q: What is the CAS number for .trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione?

The CAS number of .trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione is 26340-00-1.

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.trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione

Product Name.trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione
cas26340-00-1
purity99%

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Reputable factory supply .trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione 26340-00-1 in bulk at low price

Molecular Formula:C₁₉H₁₆N₂O₄
Molecular Weight:336.347
Vapor Pressure:3.13E-14mmHg at 25°C
Boiling Point:597.3°Cat760mmHg
PKA:-1.25±0.20(Predicted)
Flash Point:315°C
PSA：66.92000
Density:1.388g/cm³
LogP:1.82080

.trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione(Cas 26340-00-1) Usage

General Description

.trans.-1,3-dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione is a chemical compound that consists of a dibenzyl-dihydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione backbone. It is a trione compound that contains a furan ring fused to an imidazole ring, with three carbonyl groups attached to the imidazole ring. The presence of benzyl groups in the structure indicates the substitution of hydrogen atoms with benzyl groups. This chemical compound may have potential applications in pharmaceutical research and drug development due to its unique structure and potential biological activity. Further research and testing are likely required to fully understand the properties and potential uses of this compound.

InChI:InChI=1/C19H16N2O4/c22-17-15-16(18(23)25-17)21(12-14-9-5-2-6-10-14)19(24)20(15)11-13-7-3-1-4-8-13/h1-10,15-16H,11-12H2/t15-,16-/m0/s1

26340-00-1 Relevant articles

METHOD FOR PRODUCING AMIDE CARBOXYLIC ACID COMPOUND, AND METHOD FOR PRODUCING AMIDE ALCOHOL COMPOUND, AND METHOD FOR PRODUCING LACTONE COMPOUND

-

Paragraph 0100-0103, (2021/06/11)

PROBLEM TO BE SOLVED: To provide a produ...

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 stereoselectively synthesizing chiral lactone, chiral compound and application of chiral compound

-

Paragraph 0097; 0100-0101, (2021/07/17)

The invention relates to the field of or...

Method for Producing Intermediate of Biotin and Method for Producing Biotin

-

Paragraph 0331-0333; 0341, (2020/01/08)

In the method, a trione compound represe...

26340-00-1 Process route

: 108-24-7
acetic anhydride

: 51591-75-4,634188-82-2
cis-1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid

: 26339-42-4,26340-00-1
(4S,5R)-1,3-dibenzyl-1H-furo[3,4-d]imidazole-2,4,6-trione

Conditions

Conditions	Yield

: 129388-92-7
(3aR,6S,6aS)-1,3-dibenzyl-6-hydroxy-3,3a,6,6a-tetrahydro-1H-furo<3,4-d>imidazole-2,4-dione

: 26339-42-4,26340-00-1
(4S,5R)-1,3-dibenzyl-1H-furo[3,4-d]imidazole-2,4,6-trione

Conditions

Conditions	Yield
With sodium hydroxide; acetic anhydride; silver nitrate; Yield given. Multistep reaction; 1) H₂O, EtOH, r.t., 2) reflux, 5 min;

26340-00-1 Upstream products

108-24-7
acetic anhydride
51591-75-4
cis-1,3-dibenzyl-2-oxoimidazolidine-4,5-dicarboxylic acid
129388-92-7
(3aR,6S,6aS)-1,3-dibenzyl-6-hydroxy-3,3a,6,6a-tetrahydro-1H-furo<3,4-d>imidazole-2,4-dione
28092-55-9
Acetic acid (3aR,4R,6aS)-1,3-dibenzyl-2,6-dioxo-hexahydro-furo[3,4-d]imidazol-4-yl ester

26340-00-1 Downstream products

28092-55-9
6ξ-acetoxy-1,3-dibenzyl-(3ar,6ac)-tetrahydro-furo[3,4-d]imidazole-2,4-dione
87585-00-0
(4S,5R)-1,3-dibenzyl-5-hydroxymethyl-2-oxoimidazolidine-4-carboxylic acid lactone