70680-20-5

Basic information

• Product Name: 2-Butyl-5-pentylresorcinol
• Synonyms: 2-Butyl-5-pentyl-1,3-benzenediol;2-Butyl-5-pentylresorcinol;2-butyl-5-pentylbenzene-1,3-diol
• CAS NO: 70680-20-5
• Molecular Formula: C₁₅H₂₄O₂
• Molecular Weight: 236.3499
• Mol File: 70680-20-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 379.2°Cat760mmHg
• Flash Point: 174.4°C
• Appearance: /
• Density: 1.008g/cm³
• Refractive Index: 1.59
• CAS DataBase Reference: 2-Butyl-5-pentylresorcinol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butyl-5-pentylresorcinol(70680-20-5)
• EPA Substance Registry System: 2-Butyl-5-pentylresorcinol(70680-20-5)

Safety Data

• Hazardous Substances Data: 70680-20-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H18O2/c1-2-3-9-14-15(17)10-13(11-16(14)18)12-7-5-4-6-8-12/h4-8,10-11,17-18H,2-3,9H2,1H3

Upstream product

• 123-39-7 N-Methylformamide 
• 22976-40-5 1,3-dimethoxy-5-pentylbenzene 
• 106-94-5 propyl bromide 
• 126838-67-3 1,3-Dimethoxy-2-butyl-5-pentylbenzene 
• 7311-34-4 3,5-dimethoxybenzaldehdye 

Relevant articles and documents

High-Yielding Total Synthesis of Sexually Deceptive Chiloglottones and Antimicrobial Dialkylresorcinols through an Organocatalytic Reductive Coupling Reaction

Biologically important, less-explored natural products of sexually deceptive chiloglottones, antimicrobial dialkylresorcinols, and their many analogues were synthesized in very good yields in a sequential two-pot manner by using an "organocatalytic reductive coupling reaction" as the key step. Sexually deceptive chiloglottones, antimicrobial dialkylresorcinols, and their many analogues are synthesized in very good yields in a sequential two-pot manner by using an "organocatalytic reductive coupling reaction" as the key step.

Investigations on metabolites of microorganisms, XIX. The synthesis of some antibiotically active 2,5-Dialkylresorcinols - synthesis of the antibiotics DB 2073 and stemphol

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