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1642300-95-5

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1642300-95-5 Usage

Description

(E)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)-2-bromoacrylamide is a synthetic organic molecule characterized by its complex structure. It features a 1,2,4-triazole ring connected to a bromoacrylamide group, with the double bond having an (E)-configuration. The molecule is further distinguished by the presence of two trifluoromethyl groups and a phenyl group, which contribute to its highly fluorinated and aromatic properties. This unique molecular architecture may endow it with potential applications in various fields, including medicinal chemistry, materials science, and other research areas. However, further investigation and experimentation are required to fully comprehend its characteristics and possible uses.

Uses

Used in Medicinal Chemistry:
(E)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)-2-bromoacrylamide is used as a potential candidate in medicinal chemistry for its unique structure and functional groups. The presence of the 1,2,4-triazole ring and the bromoacrylamide group may allow for interactions with biological targets, making it a promising compound for the development of new drugs.
Used in Materials Science:
In the field of materials science, (E)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)-2-bromoacrylamide is used as a building block for the synthesis of novel materials. Its highly fluorinated and aromatic nature may contribute to the development of materials with specific properties, such as enhanced stability, reactivity, or selectivity in various applications.
Used in Research Fields:
(E)-3-(3-(3,5-bis(trifluoromethyl)phenyl)-1H-1,2,4-triazol-1-yl)-2-bromoacrylamide is used as a research tool in various scientific disciplines. Its complex structure and functional groups make it an interesting subject for studying the effects of molecular architecture on chemical and physical properties, as well as for exploring its potential in catalysis, sensing, or other advanced applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1642300-95-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,4,2,3,0 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1642300-95:
(9*1)+(8*6)+(7*4)+(6*2)+(5*3)+(4*0)+(3*0)+(2*9)+(1*5)=135
135 % 10 = 5
So 1642300-95-5 is a valid CAS Registry Number.

1642300-95-5Relevant articles and documents

NUCLEAR TRANSPORT MODULATORS AND USES THEREOF

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Paragraph 00337, (2015/01/07)

The present invention relates to compounds of formula (I): and pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising the compounds of formula (I) or their pharmaceutically acceptable salts, and methods of using said compounds, salts and compositions in the treatment of various disorders associated with CRM1 activity.

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