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"Benzenamine, 4-(3,3,3-trifluoro-1-propenyl)-" is a chemical compound with the molecular formula C9H8F3N. It is an aromatic amine derivative, characterized by the presence of a benzene ring with an amine group (-NH2) at the 4-position and a 3,3,3-trifluoro-1-propenyl group attached to it. Benzenamine, 4-(3,3,3-trifluoro-1-propenyl)- is known for its unique properties, such as its reactivity and potential applications in the synthesis of pharmaceuticals and other organic compounds. Due to the presence of fluorine atoms, it exhibits enhanced lipophilicity and metabolic stability, which can be advantageous in drug design. The compound is also of interest in materials science for its potential use in the development of new polymers and coatings."

1983-15-9

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1983-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1983-15-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1983-15:
(6*1)+(5*9)+(4*8)+(3*3)+(2*1)+(1*5)=99
99 % 10 = 9
So 1983-15-9 is a valid CAS Registry Number.

1983-15-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(3,3,3-trifluoroprop-1-enyl)aniline

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:1983-15-9 SDS

1983-15-9Relevant academic research and scientific papers

Deoxofluorination of (Hetero)aromatic Acids

Alekseenko, Anatoliy N.,Bugera, Maksym Ya.,Gerus, Igor I.,Kiriakov, Oleksandr,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Pustovit, Yurii,Razhyk, Bohdan,Semenov, Sergey,Starova, Viktoriia S.,Tananaiko, Oksana Yu.,Tarasenko, Karen,Tolmachev, Andrei A.,Trofymchuk, Serhii,Zaporozhets, Olga A.

, p. 3110 - 3124 (2020/03/23)

Diverse trifluoromethyl-substituted compounds were synthesized by deoxofluorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride. The obtained products were used as starting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building blocks for medicinal chemistry and agrochemistry.

Hydrolysis of hydroxybenzotrifluorides and fluorinated uracil derivatives. A general mechanism for carbon fluorine bond labilization

Sakai,Santi

, p. 1079 - 1084 (2007/10/09)

The kinetics of hydrolysis of o and p hydroxybenzotrifluoride (1 and 2) and 1 trifluoromethyl 2 (4 hydroxyphenyl) ethylene (3) and the uracil derivatives 5 difluoromethyluracil (5) and 1 methyl 5 difluoromethyluracil (6) are described. Compounds 1 and 2 h

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