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3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]--Cyclobutene-1,2-dione is a synthetic intermediate with a cyclobutene-1,2-dione core structure, featuring an aminophenyl group with trifluoromethyl substituents and a cyclohexylamine group with dimethylamino substituents. It is classified as a cyclic amine and carbonyl compound, and is used in chemical research and drug development processes.

1211565-07-9

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1211565-07-9 Usage

Uses

Used in Pharmaceutical Industry:
3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]--Cyclobutene-1,2-dione is used as a synthetic intermediate for the production of pharmaceuticals and other organic compounds. Its unique chemical structure and properties make it versatile for use in various chemical reactions and synthesis processes, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Research:
3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]--Cyclobutene-1,2-dione is used as a research compound in chemical research, where its properties and reactivity are studied to gain insights into the behavior of similar compounds and to develop new synthetic methods and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1211565-07-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,6 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1211565-07:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*6)+(3*5)+(2*0)+(1*7)=109
109 % 10 = 9
So 1211565-07-9 is a valid CAS Registry Number.

1211565-07-9SDS

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 3-((3,5-bis(trifluoromethyl)phenyl)amino)-4-(((1R,2R)-2-(dimethylamino)cyclohexyl)amino)cyclobut-3-ene-1,2-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:1211565-07-9 SDS

1211565-07-9Downstream Products

1211565-07-9Relevant academic research and scientific papers

Enantioselective α-amination of 1,3-dicarbonyl compounds using squaramide derivatives as hydrogen bonding catalysts

Konishi, Hideyuki,Lam, Tin Yiu,Malerich, Jeremiah P.,Rawal, Viresh H.

, p. 2028 - 2031 (2010)

Figure presented Catalytic enantioselective α-hydrazination of 1,3-dicarbonyl compounds with azodicarboxylates was investigated in the presence of our newly developed hydrogen bonding catalyst, squaramide 3j. High yields and high enantioselectivities were

A New Class of Squaramide-Containing Phase-Transfer Catalysts: Application to Asymmetric Fluorination of β-Keto Esters

Wang, Bin,He, Yingdong,Fu, Xuancheng,Wei, Zhonglin,Lin, Yingjie,Duan, Haifeng

, p. 2588 - 2592 (2015)

The squaramide moiety has proven to be a powerful hydrogen-bonding donor in organocatalysis, but chiral phase-transfer catalysts bearing the squaramide motif have not been reported so far. Reported herein is this kind of catalyst and their catalytic performance in the asymmetric fluorination of β-keto esters.

ONE-POT SYNTHESIS OF SQUARAMIDES

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Page/Page column 10; 14; 41, (2016/01/25)

The present invention refers to the first one-pot synthesis of squaramides. The one-pot synthesis of squaramides described herein is an easy and straightforward procedure to obtain squaramide derivatives which saves energy, avoids time consuming purificat

Squaramide-catalyzed enantioselective Friedel-Crafts reaction of indoles with imines

Qian, Yong,Ma, Gaoyuan,Lv, Aifeng,Zhu, Hai-Liang,Zhao, Jing,Rawal, Viresh H.

supporting information; experimental part, p. 3004 - 3006 (2010/08/05)

Chiral squaramides are highly enantioselective catalysts for Friedel-Crafts reaction of indoles with N-tosyl imines, affording 3-indolyl methanamine products in 85-96% yields and 84-96% ees. The Royal Society of Chemistry 2010.

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