75500-04-8

Basic information

• Product Name: 1,3-dibenzyldihydropyrimidine-2,4(1H,3H)-dione
• Synonyms: 1,3-dibenzyldihydropyrimidine-2,4(1H,3H)-dione
• CAS NO: 75500-04-8
• Molecular Weight: 294.353
• Mol File: 75500-04-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,3-dibenzyldihydropyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dibenzyldihydropyrimidine-2,4(1H,3H)-dione(75500-04-8)
• EPA Substance Registry System: 1,3-dibenzyldihydropyrimidine-2,4(1H,3H)-dione(75500-04-8)

Safety Data

• Hazardous Substances Data: 75500-04-8(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 504-07-4 5,6-dhydrouracil 
• 34001-56-4 1,3-dibenzyluracil 

Downstream Products

• 532413-11-9 (R)-1,3-Dibenzyl-5-[(S)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-dihydro-pyrimidine-2,4-dione 
• 532413-10-8 (S)-1,3-Dibenzyl-5-[(S)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-dihydro-pyrimidine-2,4-dione 
• 532413-12-0 (R)-1,3-Dibenzyl-5-[(S)-(tert-butyl-dimethyl-silanyloxy)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-dihydro-pyrimidine-2,4-dione 
• 532413-13-1 (S)-1,3-Dibenzyl-5-[(S)-(tert-butyl-dimethyl-silanyloxy)-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-methyl]-dihydro-pyrimidine-2,4-dione 

Relevant articles and documents

Iridium-Catalyzed β-C(sp2)?H Borylation of Enamides – Access to 3,3-Dihalogeno-2-methoxypiperidines

An efficient catalytic preparation of synthetically useful new β-borylated enamides was achieved under relatively mild conditions via a regioselective iridium-catalyzed C(sp2)?H borylation. The method features broad substrate scope, good functi

Use of 1,3-dibenzyl-dihydrouracil in the chain extension of 2,3-O-isopropylidene-D-glyceraldehyde

The aldol-type addition of 1,3-dibenzyl-dihydrouracil 2 to 2,3-O-isopropylidene-D-glyceraldehyde 3 was examined in different solvents and under Lewis acid catalysis in order to establish the stereochemical preferences. A stereodivergent synthesis of 5-trihydroxypropyl-dihydrouracil derivatives 4 and its C-5 epimer 5 was realized. The synthesis of ureido polyols 8 and 10 was obtained via the reductive ring opening of the templates 4 and 5.

The preparation of 1-allyluracil. N(1)-alkylation of N(3)-protected uracil derivatives

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