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13909-07-4

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13909-07-4 Usage

Structure

A synthetic compound with a trifluoroethyl group attached to an isoindole-1,3(2H)-dione core

Usage

Building block for the synthesis of various pharmaceuticals and agrochemicals, reagent in chemical reactions, development of new materials

Uniqueness

Unique structure and functional groups make it a valuable tool for the discovery and development of novel compounds with potential biological and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13909-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13909-07:
(7*1)+(6*3)+(5*9)+(4*0)+(3*9)+(2*0)+(1*7)=104
104 % 10 = 4
So 13909-07-4 is a valid CAS Registry Number.

13909-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,2,2-trifluoroethyl)isoindoline-1,3-dione

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:13909-07-4 SDS

13909-07-4Downstream Products

13909-07-4Relevant articles and documents

Efficient palladium-catalyzed double carbonylation of o-dibromobenzenes: Synthesis of thalidomide

Chen, Jianbin,Natte, Kishore,Spannenberg, Anke,Neumann, Helfried,Beller, Matthias,Wu, Xiao-Feng

, p. 5578 - 5581 (2014)

We describe here a convenient and mild procedure for double carbonylation of o-dibromobenzenes with various 2-amino pyridines and naturally occurring amines, thus providing in good to excellent yields N-substituted phthalimides by using this palladium-catalyzed carbonylation procedure. Furthermore, for the first time we have applied the developed synthetic protocol for the synthesis of biologically active molecule thalidomide via a single step carbonylative cyclization reaction in excellent yield. the Partner Organisations 2014.

Interrupting the Barton?McCombie reaction: Aqueous deoxygenative trifluoromethylation of o-alkyl thiocarbonates

Liu, Zhi-Yun,Cook, Silas P.

, p. 808 - 813 (2021/02/01)

The site-selective trifluoromethylation of aliphatic systems remains an important challenge. This work describes a light-driven, copper-mediated trifluoromethylation of O-alkyl thiocarbonates. The reaction provides broad functional group tolerance (e.g., alkyne, alkene, phenol, free alcohol, electron-rich and -deficient arenes), thereby offering orthogonality and practicality for trifluoromethylation. A radical organometallic mechanism is proposed.

Silver-Catalyzed Decarboxylative Trifluoromethylation of Aliphatic Carboxylic Acids

Tan, Xinqiang,Liu, Zhonglin,Shen, Haigen,Zhang, Pei,Zhang, Zhenzhen,Li, Chaozhong

supporting information, p. 12430 - 12433 (2017/09/25)

The silver-catalyzed decarboxylative trifluoromethylation of aliphatic carboxylic acids is described. With AgNO3 as the catalyst and K2S2O8 as the oxidant, the reactions of aliphatic carboxylic acids with (bpy)C

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