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4-CINNAMYLPHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24126-82-7

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24126-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24126-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,2 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24126-82:
(7*2)+(6*4)+(5*1)+(4*2)+(3*6)+(2*8)+(1*2)=87
87 % 10 = 7
So 24126-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O/c16-15-11-9-14(10-12-15)8-4-7-13-5-2-1-3-6-13/h1-7,9-12,16H,8H2/b7-4+

24126-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3-phenylprop-2-enyl)phenol

1.2 Other means of identification

Product number -
Other names para-Cinnamylphenol

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:24126-82-7 SDS

24126-82-7Downstream Products

24126-82-7Relevant academic research and scientific papers

Silver(I) catalyzed intermolecular alkene carbo-alkoxylation through cleavage of allylic ether C–O bond

Chen, Bai-Ling,Wang, Yu-Jiang,Shao, Ming-Zhe,Chen, Zili

, (2020)

All rights reserved. First example of allylic ether's dimerization reaction was developed through olefin's C–O bond insertion via Ag(I) catalysis. Other aromatic olefins, such as styrene and its electro-poor analogues could participate to provide the ally

PROCESSES FOR THE PREPARATION OF ORTHO-ALLYLATED HYDROXY ARYL COMPOUNDS

-

Paragraph 00272-00273, (2021/12/08)

The present application describes process for preparing an ortho-allylated hydroxy aryl compounds such as compounds of Formula (I) by reacting an allylic alcohol with a hydroxy aryl compound in the presence of aluminum compound selected from alumina and aluminum alkoxides and in a non-protic solvent wherein at least one carbon atom ortho to the hydroxy group in the hydroxy aryl compound is unsubstituted. The present application also includes compounds of Formula (I).

Palladium-catalyzed allylic arylation of allylic ethers with arylboronic acids using hydrazone ligands

Mino, Takashi,Kogure, Taketo,Abe, Taichi,Koizumi, Tomoko,Fujita, Tsutomu,Sakamoto, Masami

, p. 1501 - 1505 (2013/05/09)

Unsymmetrical 1,3-diarylpropenes were synthesized in good to high yields by the palladium-catalyzed allylic arylation of allylic ethers, such as a cinnamyl phenyl ether, with a variety of arylboronic acids using a hydrazone 1a-Pd(OAc)2 system in DMAc/H2O. Using this catalyst, eugenol was also synthesized from allyl phenyl ether with (4-hydroxy-3- methoxyphenyl)boronic acid pinacol ester. A palladium-catalyzed allylic arylation of cinnamyl phenyl ether derivatives with a variety of arylboronic acids using 5 mol-% of a hydrazone 1a-Pd(OAc)2 system in DMAc/H 2O at 50 °C gave 1,3-diarylpropenes in good yields. We also succeeded with the synthesis of eugenol by a palladium-catalyzed allylic arylation. Copyright

Operationally simple and highly (E)-styrenyl-selective heck reactions of electronically nonbiased olefins

Werner, Erik W.,Sigman, Matthew S.

supporting information; experimental part, p. 9692 - 9695 (2011/08/06)

Simple, mild, and efficient conditions are reported for a Pd 0-catalyzed Heck reaction that delivers high yields and selectivity for (E)-styrenyl products using electronically nonbiased olefin substrates bearing a range of useful functionality. Preliminary mechanistic studies demonstrate that the σ-donating DMA solvent is crucial for high selectivity. Further studies suggest that the catalyst distinguishes between β-hydrogens on the basis of their relative hydridic character, in contrast to previously reported PdII-catalyzed oxidative reaction conditions.

Anti-staphylococcal activity and β-lactam resistance attenuating capacity of structural analogues of (-)-epicatechin gallate

Anderson, James C.,McCarthy, Robert A.,Paulin, Sarah,Taylor, Peter W.

supporting information; scheme or table, p. 6996 - 7000 (2012/01/06)

We examined the impact of gradual removal of hydroxyl groups from the A- and B-rings of (-)-epicatechin gallate on antibacterial activity and oxacillin resistance attenuation of an epidemic strain of methicillin resistant Staphylococcus aureus. Removal of

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