Welcome to LookChem.com Sign In|Join Free
  • or
4-acetyl-3-phenyl-1H-isochromen-1-one is a chemical compound with the molecular formula C17H11NO2. It is a derivative of isochromen-1-one, characterized by the presence of an acetyl group (-COCH3) at the 4-position and a phenyl group (C6H5) at the 3-position. 4-acetyl-3-phenyl-1H-isochromen-1-one is known for its potential applications in the synthesis of various pharmaceuticals and organic compounds due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions involving isochromen-1-one and phenyl acetic acid, followed by acetylation. The compound's properties, such as its solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic chemistry.

118520-80-2

Post Buying Request

118520-80-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

118520-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118520-80-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,2 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 118520-80:
(8*1)+(7*1)+(6*8)+(5*5)+(4*2)+(3*0)+(2*8)+(1*0)=112
112 % 10 = 2
So 118520-80-2 is a valid CAS Registry Number.

118520-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetyl-3-phenylisochromen-1-one

1.2 Other means of identification

Product number -
Other names 4-acetyl-3-phenyl-1h-isochromen-1-one

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:118520-80-2 SDS

118520-80-2Downstream Products

118520-80-2Relevant academic research and scientific papers

Lactonization of 2-Alkynylbenzoates for the Assembly of Isochromenones Mediated by BF3·Et2O

Zhang, Xiang,Wan, Xintong,Cong, Ying,Zhen, Xiaohua,Li, Qiao,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 10402 - 10411 (2019/08/20)

A general and efficient lactonization method of readily available 2-alkynylbenzoates affording biologically important isochromenones has been realized via a solely BF3·Et2O-mediated 6-endo-dig cyclization process under mild condition

Synthesis of 3-arylisocoumarins, including thunberginols A and B, unsymmetrical 3,4-disubstituted isocoumarins, and 3-ylidenephthalides via iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids

Rossi, Renzo,Carpita, Adriano,Bellina, Fabio,Stabile, Paolo,Mannina, Luisa

, p. 2067 - 2081 (2007/10/03)

3-Aryl-4-iodoisocoumarins, which were readily and efficiently prepared by regioselective iodolactonization of methyl 2-ynylbenzoates or the corresponding carboxylic acids, were used as precursors either to 3-arylisocoumarins, including naturally-occurring

Organomercury Mediated Synthesis of Isocoumarins

Nagarajan, A.,Balasubramanian, Tiruvenkat R.

, p. 917 - 919 (2007/10/02)

A facile and convenient synthesis of isocoumarins via an organomercurial route is reported.The synthesis involves reaction of methyl 2-alkynbenzoates with mercuric acetate to give the corresponding isocoumarin mercurials which serve as intermediates to afford the appropriate isocoumarins having substituents as Cl,I,Br,COCH3 etc.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 118520-80-2