15058-72-7

Basic information

• Product Name: IFLAB-BB F2124-0958
• Synonyms: IFLAB-BB F2124-0958;2,4-DIMETHYL-FURAN-3-CARBOXYLIC ACID;2,4-Dimethyl-3-furoic acid, 97%;3-Furancarboxylic acid, 2,4-diMethyl-
• CAS NO: 15058-72-7
• Molecular Formula: C₇H₈O₃
• Molecular Weight: 140.14
• Mol File: 15058-72-7.mol
• Article Data: 1

Chemical Properties

• Melting Point: 123 °C
• Boiling Point: 240.2±35.0 °C(Predicted)
• Appearance: /
• Density: 1.194±0.06 g/cm3(Predicted)
• PKA: 4.45±0.40(Predicted)
• CAS DataBase Reference: IFLAB-BB F2124-0958(CAS DataBase Reference)
• NIST Chemistry Reference: IFLAB-BB F2124-0958(15058-72-7)
• EPA Substance Registry System: IFLAB-BB F2124-0958(15058-72-7)

Safety Data

• Hazardous Substances Data: 15058-72-7(Hazardous Substances Data)

Usage

General Description

IFLAB-BB F2124-0958 refers to a specific chemical compound with the molecular formula C16H24N2O2. IFLAB-BB F2124-0958 is used as a chiral derivatizing reagent for the determination of amino acids and other compounds in biological samples. It is commonly employed in analytical and biochemical research, as well as in pharmaceutical development processes. IFLAB-BB F2124-0958 is known for its ability to form stable and highly fluorescent derivatives, making it a valuable tool in the analysis and quantification of various biomolecules. Its unique properties and versatile applications make it a key component in many laboratory settings.

Upstream product

• 67-56-1 methanol 
• 127395-63-5 2,4-dimethyl-3-furanylcarbonyl α-L-rhamnopyranoside 

Downstream Products

• 15139-39-6 2,4-dimethyl-furan-3-carbonyl chloride 
• 15139-38-5 2,4-Dimethyl-5-nitro-furan-3-carbonsaeure 
• 73524-14-8 4-methyl-2-(2-methyl-3-oxo-1-cyclohexenylmethyl)-3-furoic acid 
• 28730-18-9 2,4-dimethylfuran-3-carboxanilide 
• 34297-68-2 3,5-dimethyl-2-furancarboxylic acid 
• 75002-34-5 2,4-dimethyl-furan-3-carbaldehyde 
• 73524-15-9 4-methyl-2-(2-methyl-3-oxocyclohexylmethyl)-3-furoic acid 

Relevant articles and documents

Secondary metabolites by chemical screening, 39: Acyl α-L- rhamnopyranosides, a novel family of secondary metabolites from streptomyces sp.: Isolation and biosynthesis

In the course of our chemical screening program, the novel acyl α-L- rhamnopyranosides (1-6) were detected as metabolites from five different strains of Streptomycetes. The structures of all these compounds were elucidated by chemical and spectroscopic methods. The biosynthesis of 1 and 3 was established by feeding 13C-labelled acetate, glycerol, and d-glucose to Streptomyces griseoviridis (strain Tu 3634), and resulted in a complete labelling pattern of the 2,4-dimethyl-3-furanylcarbonyl and benzoyl residues, as well as the rhamnose moiety. These results reveal biosynthetic pathways of general importance and give an insight into the generation of the hexose phosphates, from which deoxysugars are formed. The acyl rhamnosides are members of a novel family of microbial metabolites and are considered as rhamnoconjugates from Streptomycetes.