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23028-23-1

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23028-23-1 Usage

Synthesis Reference(s)

Synthesis, p. 1061, 1986 DOI: 10.1055/s-1986-31877

Check Digit Verification of cas no

The CAS Registry Mumber 23028-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,2 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23028-23:
(7*2)+(6*3)+(5*0)+(4*2)+(3*8)+(2*2)+(1*3)=71
71 % 10 = 1
So 23028-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O2/c1-11-13-9-5-6-10-14(13)18-16(17)15(11)12-7-3-2-4-8-12/h2-10H,1H3

23028-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-3-phenylchromen-2-one

1.2 Other means of identification

Product number -
Other names 4-Methyl-3-phenylcoumarin

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:23028-23-1 SDS

23028-23-1Downstream Products

23028-23-1Relevant articles and documents

Multicomponent Synthesis of Iminocoumarins via Rhodium-Catalyzed C - H Bond Activation

Chen, Zhan,Jin, Shengnan,Jiang, Wenyao,Zhu, Feimin,Chen, Yuqi,Zhao, Yingwei

, p. 11006 - 11013 (2020)

We herein establish a multicomponent annulation method for the synthesis of valuable iminocoumarins using aryl thiocarbamates, internal alkynes, and sulfonamides as starting materials, which are safe and readily available. The key step is a Rh-catalyzed a

Zn(II)-Catalyzed One-Pot Synthesis of Coumarins from Ynamides and Salicylaldehydes

Yoo, Huen Ji,Youn, So Won

, p. 3422 - 3426 (2019/05/10)

A highly efficient and straightforward synthesis of diversely substituted coumarins from ynamides and salicylaldehydes in the presence of Zn(II) catalyst has been developed. The sulfonamide moiety of ynamides was successfully recycled in this process, serving as an effective traceless directing group for high regioselectivity in the bond-forming event. The advantages of this protocol are good functional group tolerance, broad substrate scope, simple and high-yielding reaction, recovery/reuse of the sulfonamides, low catalyst loading of inexpensive catalyst, and, by these merits, a more cost-effective and greener process.

Ph3P/I2-Mediated Synthesis of 3-Aryl-Substituted and 3,4-Disubstituted Coumarins

Phakhodee, Wong,Duangkamol, Chuthamat,Yamano, Dolnapa,Pattarawarapan, Mookda

, p. 825 - 830 (2017/04/06)

Ph3P/I2-Et3N-mediated one-pot two-step esterification-cyclization toward 3-aryl coumarins and 3-aryl-4-methylcoumarins is reported. The reaction of a variety of aryl acetic acids containing steric or reactive group with 2-

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