7154-01-0

Basic information

• Product Name: Safrolglycol
• Synonyms: Safrolglycol;2',3'-Dihydro-2',3'-dihydroxysafrole;3-(3,4-Methylenedioxyphenyl)-1,2-propanediol;NSC 43297;3-(Benzo[d][1,3]dioxol-5-yl)propane-1,2-diol
• CAS NO: 7154-01-0
• Molecular Formula: C₁₀H₁₂O₄
• Molecular Weight: 196.19988
• Mol File: 7154-01-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 69 °C
• Boiling Point: 392.5°Cat760mmHg
• Flash Point: 191.2°C
• Appearance: /
• Density: 1.35g/cm³
• Vapor Pressure: 7.28E-07mmHg at 25°C
• Refractive Index: 1.598
• PKA: 14.12±0.20(Predicted)
• CAS DataBase Reference: Safrolglycol(CAS DataBase Reference)
• NIST Chemistry Reference: Safrolglycol(7154-01-0)
• EPA Substance Registry System: Safrolglycol(7154-01-0)

Safety Data

• Hazardous Substances Data: 7154-01-0(Hazardous Substances Data)

Usage

General Description

Safrolglycol is a chemical compound that is commonly used in the production of perfumes and fragrances. It is a colorless to pale yellow liquid that has a floral, sweet, and spicy aroma. Safrolglycol is often utilized as a fragrance ingredient in a wide range of personal care products, including soaps, lotions, and cosmetics. In addition to its aromatic properties, safrolglycol also has solvent properties and can be used in various industrial applications. However,

InChI:InChI=1/C10H12O4/c11-5-8(12)3-7-1-2-9-10(4-7)14-6-13-9/h1-2,4,8,11-12H,3,5-6H2

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Relevant articles and documents

Site-Selective Mono-Oxidation of 1,2-Bis(boronates)

Site-selective oxidation of vicinal bis(boronates) is accomplished through the use of trimethylamine N-oxide in 1-butanol solvent. The reaction occurs with good efficiency and selectivity across a range of substrates, providing 2-hydro-1-boronic esters which are shown to be versatile intermediates in the synthesis of chiral building blocks.

LITHIATION OF THE BENZENE RING IN THE PRESENCE OF ortho-ALKYL SUBSTITUENTS BEARING ONE OR TWO HETEROATOMS ON THE β-CARBON. A CONVENIENT SYNTHESIS OF MELLEIN AND KIGELIN

The title reaction can be successfully accomplished by proton-metal exchange with n-butyllithium, and the usually observed elimination to a styrene derivative suppressed, provided an appropriate combination of heteroatoms bound to the β-carbon of the alky