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Phenol, 4-[3-(acetyloxy)-1-propenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124389-48-6

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124389-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124389-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,8 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124389-48:
(8*1)+(7*2)+(6*4)+(5*3)+(4*8)+(3*9)+(2*4)+(1*8)=136
136 % 10 = 6
So 124389-48-6 is a valid CAS Registry Number.

124389-48-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-hydroxyphenyl)prop-2-enyl acetate

1.2 Other means of identification

Product number -
Other names Phenol,4-[3-(acetyloxy)-1-propenyl]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:124389-48-6 SDS

124389-48-6Relevant academic research and scientific papers

Preparation of monolignol γ-acetate, γ-p-hydroxycinnamate, and γ-p-hydroxybenzoate conjugates: Selective deacylation of phenolic acetates with hydrazine acetate

Zhu, Yimin,Regner, Matthew,Lu, Fachuang,Kim, Hoon,Mohammadi, Allison,Pearson, Timothy J.,Ralph, John

, p. 21964 - 21971 (2013/11/06)

We report here a reliable and facile synthesis of a range of monolignol γ-p-hydroxycinnamate (including p-coumarate, ferulate, and caffeate), γ-acetate, and γ-p-hydroxybenzoate conjugates, many not previously reported, that are either putative intermediat

DFRC Method for Lignin Analysis. 1. New Method for β-Aryl Ether Cleavage: Lignin Model Studies

Lu, Fachuang,Ralph, John

, p. 4655 - 4660 (2007/10/03)

A new method for selective and efficient cleavage of arylglycerol-β-aryl (β-O-4) ether linkages in lignins is described and applied to several lignin β-ether models. The term "DFRC" was coined for derivatization followed by reductive cleavage. Derivatization, accompanied by cell wall solubilization, is accomplished with acetyl bromide (AcBr); reductive cleavage of resulting β-bromo ethers utilizes zinc in acetic acid. Degradation monomers, 4-acetoxycinnamyl acetates, from β-ether cleavage by the DFRC method were identified by NMR, GC-MS, and comparison of GC retention times with authentic compounds. Under the conditions used in this study, the β-ether linkage of all models was cleaved in very high (>92%) yield. The DFRC method produces simpler mixtures of monomers with higher yields than alternative hydrolytic methods. Because of its relative simplicity, mild conditions, and exceptional selectivity, this method should become a powerful analytical method for lignin characterization.

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