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1211565-07-9

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  • 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]-3-cyclobutene-1,2-dione, 98%, (99% ee)

    Cas No: 1211565-07-9

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  • 3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(1R,2R)-2-(dimethylamino)cyclohexyl]amino]-3-cyclobutene-1,2-dione

    Cas No: 1211565-07-9

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1211565-07-9 Usage

General Description

The chemical 3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]--Cyclobutene-1,2-dione is a compound with a cyclobutene-1,2-dione core structure and contains an aminophenyl group with trifluoromethyl substituents, as well as a cyclohexylamine group with dimethylamino substituents. 3-[[3,5-bis(trifluoroMethyl)phenyl]aMino]-4-[[(1R,2R)-2-(diMethylaMino)cyclohexyl]aMino]--Cyclobutene-1,2-dione is a synthetic intermediate used in the production of pharmaceuticals and other organic compounds. It is classified as a cyclic amine and carbonyl compound and is used in chemical research and drug development processes. Its chemical structure and properties make it versatile for use in various chemical reactions and synthesis processes.

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

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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 articles and documents

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

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

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