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60125-23-7

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60125-23-7 Usage

General Description

3-(2-Hydroxyphenyl)-2-propenal, also known as 3-(2-hydroxyphenyl)acrolein, is a chemical compound with the molecular formula C9H8O2. It is a yellow liquid with a strong, sweet odor and is commonly used in the production of fragrances and flavorings. 3-(2-Hydroxyphenyl)-2-propenal is also a type of alpha,beta-unsaturated aldehyde, making it a reactive compound that can undergo a variety of chemical reactions. It is important to handle this chemical with caution as it can be irritating to the skin, eyes, and respiratory system, and may also be harmful if ingested or inhaled in large quantities. Additionally, 3-(2-Hydroxyphenyl)-2-propenal is known to have potential mutagenic and cytotoxic effects, and should be handled with appropriate safety measures in place.

Check Digit Verification of cas no

The CAS Registry Mumber 60125-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,2 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60125-23:
(7*6)+(6*0)+(5*1)+(4*2)+(3*5)+(2*2)+(1*3)=77
77 % 10 = 7
So 60125-23-7 is a valid CAS Registry Number.

60125-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-Hydroxyphenyl)acrylaldehyde

1.2 Other means of identification

Product number -
Other names -

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:60125-23-7 SDS

60125-23-7Relevant articles and documents

Synthesis of Diarylheptanoid Scaffolds Inspired by Calyxins i and J

Ackrill, Thomas D.,Sparkes, Hazel A.,Willis, Christine L.

, p. 3884 - 3887 (2015)

Unsaturated alcohols are prepared efficiently in two steps from o-hydroxycinnamaldehyde. The TMSOTf-mediated reaction of the γunsaturated alcohols with aldehydes creates two oxygen heterocycles and three new stereocenters in a single pot. The approach is

Method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and diphosphine ligand used in method

-

Paragraph 0163; 0164, (2021/05/29)

The invention discloses a method for preparing olefine aldehyde by catalyzing terminal alkyne or terminal conjugated eneyne and a diphosphine ligand used in the method. According to the invention, indole-substituted phosphoramidite diphosphine ligand which is stable in air and insensitive to light is synthesized by utilizing a continuous one-pot method, and the indole-substituted phosphoramidite diphosphine ligand and a rhodium catalyst are used for jointly catalyzing to successfully achieve a hydroformylation reaction of aromatic terminal alkyne and terminal conjugated eneyne under the condition of synthesis gas for the first time, so that an olefine aldehyde structure compound can be rapidly and massively prepared, and particularly, a polyolefine aldehyde structure compound which is more difficult to synthesize in the prior art can be easily prepared and synthesized, and a novel method is provided for synthesis and modification of drug molecules, intermediates and chemical products.

Kinetic Resolution and Dynamic Kinetic Resolution of Chromene by Rhodium-Catalyzed Asymmetric Hydroarylation

Yang, Qingjing,Wang, Yanbo,Luo, Shihui,Wang, Jun (Joelle)

supporting information, p. 5343 - 5347 (2019/03/21)

A highly efficient kinetic resolution and dynamic kinetic resolution of chromene is reported for the first time and they procced by a rhodium-catalyzed asymmetric hydroarylation pathway. This new approach offers versatile access to various chiral 2,3-diaryl-chromanes containing vicinal stereogenic centers, as well as the recovered chiral flavenes, in high yields with excellent ee values (s factor up to 532). Particularly noteworthy is that this strategy can be further extended to the establishment of a dynamic version of the kinetic resolution of chromene acetals and allows complete access to chiral isoflavanes and α-aryl hydrocoumarins.

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