78795-27-4

Usage

Synonyms

Vitamin B2

Chemical Structure

A complex molecule consisting of a pyrimidine ring fused to a cyclopentane ring, with various functional groups including hydroxyl, methyl, and carbonyl groups.

Solubility

Water-soluble

Function

Essential for various bodily functions, including energy production, metabolism, and the formation of red blood cells.

Antioxidant Properties

Helps protect cells from oxidative damage.

Food Sources

Found in a variety of foods, such as dairy products, meat, and green leafy vegetables.

Dietary Supplement

Available as a dietary supplement.

Deficiency Symptoms

Fatigue, anemia, and skin disorders.

Upstream product

• 132151-65-6 (E)-3-methoxy-2-methylacryloyl isocyanate 
• 62138-01-6 (+/-)-(1α,2α,3β,5β)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol 
• 117604-70-3 (+)-1-<(1α,2β,3β,4α)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl>-5-methyl-2,4-(1H,3H)pyrimidinedione 
• 78795-22-9 (+)-N-<<(1α,2β,3β,4α)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl>aminocarbonyl>-3-methoxy-2-methyl-2-propenamide 
• 116856-49-6 aza-bicyclo<2.2.1><(dimethylmethylene)dioxy-trans-5,6>-one-3-heptane 
• 78795-22-9 (+/-)-N-<<(1α,2β,3β,4α)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl>aminocarbonyl>-3-methoxy-2-methyl-2-propenamide 
• 85026-59-1 (-)-(1R,2R,3S,4R)-4-amino-2,3-dihydroxy-1-(hydroxymethyl)cyclopentane 
• 77745-22-3 exo-cis-5,6-Dihydroxy-2-azabicyclo<2.2.1>heptan-3-one 
• 117538-44-0 2,2'-anhydro-5-methyl-carbocyclic uridine 

Relevant academic research and scientific papers

Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams

Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no

SYNTHESIS OF (+)-1--5-METHYL-2,4-(1H,3H)PYRIMIDINEDIONE, THE CARBOCYCLIC ANALOGUE OF ARA-T

Compound 1, the carbocyclic analogue of Ara-T, was synthesized by a four-step synthesis from (+)-(1α,2α,3β,5β)-3-amino-5-(hydroxymethyl)-1,2-cyclopentanediol (2), which was prepared from cyclopentadiene via a eigght-step route as a potential antivirial agent.

Carbocyclic Analogs of Thymine Nucleosides and Related 1-Substituted Thymines

The carbocyclic analogs of thymidine (IXf), 1-β-ribofuranosylthymine (IXg), and 1-β-3'-deoxyribofuranosylthymine (IXe) were synthesized by incorporating modifications into the Shaw method of synthesizing 2,4-(1H,3H)pyrimidinediones via acryloylureas.Simpler analogs of thymine nucleosides were also prepared by this method.The carbocyclic analog of thymidine displayed modest activity against Leukemia L1210 in vivo.It differs from a compound prepared previously by a Prins reaction.