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55204-36-9

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55204-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55204-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55204-36:
(7*5)+(6*5)+(5*2)+(4*0)+(3*4)+(2*3)+(1*6)=99
99 % 10 = 9
So 55204-36-9 is a valid CAS Registry Number.

55204-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-N-(2,2,2-trifluoroethyl)aniline

1.2 Other means of identification

Product number -
Other names N-Ethyl-N-(trifluor-2,2,2-ethyl)anilin

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:55204-36-9 SDS

55204-36-9Relevant articles and documents

Direct N-Alkylation/Fluoroalkylation of Amines Using Carboxylic Acids via Transition-Metal-Free Catalysis

Lu, Chunlei,Qiu, Zetian,Xuan, Maojie,Huang, Yan,Lou, Yongjia,Zhu, Yiling,Shen, Hao,Lin, Bo-Lin

supporting information, p. 4151 - 4158 (2020/08/21)

A scalable protocol of direct N-mono/di-alkyl/fluoroalkylation of primary/secondary amines has been constructed with various carboxylic acids as coupling agents under the catalysis of a simple air-tolerant inorganic salt, K3PO4. Advantageous features include 100 examples, 10 drugs and drug-like amines, fluorinated complex tertiary amines, gram-scale synthesis and isotope-labelling amine, thus demonstrating the potential applicability in industry of this methodology. The involvement of relatively less reactive silicon-hydride compared with the traditional reactive metal-hydride or boron-hydride species required to reduce the amide intermediates presumably contributes to the remarkable functional group compatibility. (Figure presented.).

Fluoroalkylaryliodonuim compounds

-

, (2008/06/13)

Fluoroalkylaryliodonium compounds having the formula (I): STR1 wherein AR, A and Rf are as defined above, are disclosed. The fluoroalkylaryliodonium compounds of the present invention are useful as intermediates for producing N-fluoroalkylanilines or deri

Process for dyeing synthetic fibers formed from aromatic polyesters and new monoazo dyestuffs useful for such dyeing

-

, (2008/06/13)

The dyeing of synthetic polyester fibers wherein the dyestuff is a mono-azo dyestuff of the formula STR1 in which X represents a hydrogen, chlorine, bromine, cyano, nitro or lower alkylsulphonyl radical, R1 represents hydrogen, chlorine or bromine atom or a lower alkyl, lower alkoxy or acylamino radical, R2 represents a hydrogen atom or a lower alkoxy radical and R3 represents a lower alkyl, β -hydroxyethyl, β-cyanoethyl, β-acetoxyethyl or β-(β-acetoxyethoxy)-ethyl group.

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