Welcome to LookChem.com Sign In|Join Free
  • or
2H-Isoindole, 1-phenyl-, also known as 1-phenyl-2H-isoindole or 1-phenyl-2,3-dihydroindole, is an organic compound with the molecular formula C14H11N. It is a derivative of isoindole, a heterocyclic aromatic compound consisting of a benzene ring fused to a dihydroindole ring. The phenyl group is attached to the nitrogen atom at the 1-position, making it a substituted isoindole. 2H-Isoindole, 1-phenyl- is of interest in organic chemistry and medicinal chemistry due to its potential applications in the synthesis of various pharmaceuticals and agrochemicals. It can be synthesized through various methods, such as the condensation of o-phenylenediamine with α-ketoesters or the intramolecular cyclization of o-aminobenzaldehydes with α-bromoesters. The compound's properties, such as its reactivity and stability, make it a valuable building block for the development of new molecules with specific biological activities.

19023-49-5

Post Buying Request

19023-49-5 Suppliers

Recommended suppliers

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

19023-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19023-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,2 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19023-49:
(7*1)+(6*9)+(5*0)+(4*2)+(3*3)+(2*4)+(1*9)=95
95 % 10 = 5
So 19023-49-5 is a valid CAS Registry Number.

19023-49-5SDS

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 1-phenyl-2H-isoindole

1.2 Other means of identification

Product number -
Other names 1-Phenylisoindol

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:19023-49-5 SDS

19023-49-5Upstream product

19023-49-5Relevant academic research and scientific papers

Rh(III)-Catalyzed Coupling of N-Chloroimines with α-Diazo-α-phosphonoacetates for the Synthesis of 2 H-Isoindoles

Qi, Bing,Li, Lei,Wang, Qi,Zhang, Wenjing,Fang, Lili,Zhu, Jin

supporting information, p. 6860 - 6863 (2019/09/12)

We report herein the first use of N-chloroimines as effective synthons for directed C-H functionalization. Rh(III)-catalyzed coupling of N-chloroimines with α-diazo-α-phosphonoacetates allows for efficient dechlorinative/dephosphonative access to 2H-isoindoles. Further deesterification under Ni(II) catalysis enables the complete elimination of reactivity-assisting groups and full exposure of reactivity of C3 and N2 ring atoms for attaching structurally distinct appendages.

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 19023-49-5