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22280-95-1

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22280-95-1 Usage

General Description

4-(allyloxy)-3-methoxybenzaldehyde is a chemical compound with a molecular formula C11H12O3. It is a benzaldehyde derivative that contains an allyloxy group and a methoxy group, which are both attached to the benzene ring. This chemical is used in various industries, including pharmaceuticals and perfumery, due to its ability to act as a versatile building block in organic synthesis. It is commonly used as a reagent in organic reactions to introduce the allyloxy and methoxy groups into different molecules. The compound has a yellowish to brownish appearance and has a strong, sweet almond-like odor. Additionally, it is important to handle this chemical with care, as it can be a skin and eye irritant.

Check Digit Verification of cas no

The CAS Registry Mumber 22280-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22280-95:
(7*2)+(6*2)+(5*2)+(4*8)+(3*0)+(2*9)+(1*5)=91
91 % 10 = 1
So 22280-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-3-6-14-10-5-4-9(8-12)7-11(10)13-2/h3-5,7-8H,1,6H2,2H3

22280-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methoxy-4-prop-2-enoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names O-allylvanillin

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:22280-95-1 SDS

22280-95-1Relevant articles and documents

A concise synthesis of (±)-methoxyfumimycin ethyl ester

Zhou, Zhiwang,Hu, Yu,Wang, Bin,He, Xiaoru,Ren, Gang,Feng, Lihua

, p. 378 - 380 (2014)

The protecting-group-free synthesis of (±)-methoxyfumimycin ethyl ester, a potential bacterial peptide deformylase (PDF) inhibitor, is reported. The synthetic approach features a tandem Friedel-Crafts alkylation/lactonisation access as a key reaction to g

Design, synthesis, characterization, and anticancer activity of a novel series of O-substituted chalcone derivatives

Ngameni, Bathélémy,Cedric, Kamdoum,Mbaveng, Armelle T.,Erdo?an, Musa,Simo, Ingrid,Kuete, Victor,Da?tan, Arif

, (2021)

A new series of O-substituted chalcone derivatives bearing an/a allyl-, prenyl- or propargyl-substituent at different positions of rings A and B and their derivatives as drug leads, was designed, synthesized, and characterized. The chalcone derivatives we

Introducing the Tishchenko reaction into sustainable polymer chemistry

Ren, Tianhua,Chen, Qin,Zhao, Changbo,Zheng, Qiang,Xie, Haibo,North, Michael

, p. 1542 - 1547 (2020)

Taking advantage of the structural characteristics of lignin-derived phenolic compounds, a combination of the Williamson and Tishchenko reactions produced a series of new α,ω-diene functionalized carboxylic ester monomers from both petrochemical and renewable resources, which were applicable in subsequent thiol-ene click and acyclic diene metathesis (ADMET) polymerizations, providing a series of poly(thioether esters) and unsaturated aromatic-aliphatic polyesters with high molecular weights.

Synthesis of the intermediate for fumimycin: A natural peptide deformylase inhibitor

Zhou, Zhi-Wang,Li, Wei-Chao,Hu, Yu,Wang, Bin,Ren, Gang,Feng, Li-Hua

, p. 3049 - 3054 (2013)

Synthetic efforts toward the potential bacterial peptide deformylase inhibitor fumimycin are reported. The synthetic approach features a tandem Friedel-Crafts alkylation/lactonization access as key reaction to the α, α-disubstituted amino acid unit, and r

Chemoselective and ligand-free aerobic oxidation of benzylic alcohols to carbonyl compounds using alumina-supported mesoporous nickel nanoparticle as an efficient recyclable heterogeneous catalyst

Das, Asit Kumar,Nandy, Sneha,Bhar, Sanjay

, (2021/05/10)

An economically efficient and operationally simple ligand-free protocol for the chemoselective oxidation of benzylic alcohols to carbonyl compounds has been developed using alumina-supported nickel nanoparticles as a stable recyclable heterogeneous catalyst along with potassium tert-butoxide in the presence of aerial oxygen as an eco-friendly oxidant. The aliphatic alcohols remained unaffected under the present condition. Excellent chemoselectivity has also been demonstrated through intermolecular and intramolecular competition experiments. This protocol accommodates a diverse range of substituents with the tolerance of various sensitive moieties during the reaction. The catalyst could be recovered by filtration and reused consecutively without any significant loss in the catalytic activity. Moreover, the heterogeneity of the catalyst has also been established by the “hot filtration method (Sheldon's test)”.

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