56915-87-8

Basic information

• Product Name: TIMTEC-BB SBB000702
• Synonyms: TIMTEC-BB SBB000702;N-(3-Acetylphenyl)-2,2,2-trifluoroacetamide;3'-Acetyl-2,2,2-trifluoroacetanilide;Acetamide, N-(3-acetylphenyl)-2,2,2-trifluoro-;Acetanilide, 3'-acetyl-2,2,2-trifluoro-;Brn 3054640;BIM-0017508.P001;CBMicro_017507
• CAS NO: 56915-87-8
• Molecular Formula: C₁₀H₈F₃NO₂
• Molecular Weight: 231.17
• Mol File: 56915-87-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 325.1°C at 760 mmHg
• Flash Point: 150.4°C
• Appearance: /
• Density: 1.356g/cm³
• Vapor Pressure: 0.000235mmHg at 25°C
• Refractive Index: 1.51
• Storage Temp.: 2-8°C
• CAS DataBase Reference: TIMTEC-BB SBB000702(CAS DataBase Reference)
• NIST Chemistry Reference: TIMTEC-BB SBB000702(56915-87-8)
• EPA Substance Registry System: TIMTEC-BB SBB000702(56915-87-8)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 56915-87-8(Hazardous Substances Data)

Usage

General Description

TIMTEC-BB SBB000702 is a chemical with the molecular formula C21H44N2O4S. It is a compound with a molecular weight of 416.65 g/mol and a melting point of 64-66°C. This chemical is used in the pharmaceutical and research industries, and it is known for its properties as an anesthetic and analgesic. It is a quaternary ammonium compound and has been studied for its potential applications in various medical and scientific fields. Additionally, it is used in the synthesis of other chemical compounds and as a reference standard in analytical testing.

InChI:InChI=1/C10H8F3NO2/c1-6(15)7-3-2-4-8(5-7)14-9(16)10(11,12)13/h2-5H,1H3,(H,14,16)

Upstream product

• 137550-67-5 2,2,2-trifluoro-N-(3-(4,4,4-trifluoro-3-oxobutanoyl)phenyl)acetamide 
• 354-32-5 trifluoracetyl chloride 
• 99-03-6 1-(3-aminophenyl)ethanone 
• 431-47-0 trifluoroacetic acid-methyl ester 
• 407-25-0 trifluoroacetic anhydride 

Downstream Products

• 137550-67-5 2,2,2-trifluoro-N-(3-(4,4,4-trifluoro-3-oxobutanoyl)phenyl)acetamide 
• 844679-69-2 3-(dimetylamino)-1-[3-(methylamino) phenyl]prop-2-en-1-one 
• 134812-22-9 1-Ethyl-4-oxo-7-(2-phenyl-thiazol-4-yl)-1,4-dihydro-quinoline-3-carboxylic acid 
• 134812-04-7 diethyl 3-(2-methyl-1,3-dioxolan-2-yl)anilinomethylenemalonate 
• 134812-12-7 diethyl N-ethyl-3-acetylanilinomethylenemalonate 
• 51226-14-3 2-(3-amino)phenyl-2-methyl-1,3-dioxolane 
• 134812-13-8 3'-ethylaminoacetophenone 
• 134812-02-5 2-methyl-2-(3-trifluoroacetylamino)phenyl-1,3-dioxolane 
• 861611-98-5 1-(2-nitroamino-phenyl)-ethanone 

Relevant articles and documents

3-Trifluoroacetamidobenzoyltrifluoroacetone and its europium complexes

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Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: From potent activators to highly efficient inhibitors

In this study, we developed 3-/4-aminoacetophenones and their structure-based 3-/4-aminophenylethylidenethiosemicarbazide derivatives, respectively, as novel tyrosinase activators and inhibitors. Notably, all the obtained thiosemicarbazones displayed more potent tyrosinase inhibitory activities than kojic acid. Especially, compound 7k was found to be the most active tyrosinase inhibitor with IC50 value of 0.291 1/4M. The structure-activity relationships (SARs) analysis showed that: (1) the amine group was absolutely necessarily for determining the tyrosinase activation activity; (2) the introduction of thiosemicarbazide group played a very vital role in transforming tyrosinase activators into tyrosinase inhibitors; (3) the phenylethylenethiosemicarbazide moiety was crucial for determining the tyrosinase inhibitory activity; (4) the type of acyl group had no obvious effect on the inhibitory activity; (5) the position of amide substituent on the phenyl ring influenced the tyrosinase inhibitory potency. Moreover, the inhibition mechanism and inhibition kinetics study revealed that compound 7k was reversible and non-competitive inhibitor, and compound 8h was reversible and competitive-uncompetitive mixed-II type inhibitor.

Photolabile compound and substrate for oligomer probe array with the same

Provided is a substrate for an oligomer probe array to which a photolabile material having an acetylene derivative is directly attached or attached via a linker.