2633-50-3

Basic information

• Product Name: 2-BROMO-1-(3,4-DIMETHYL-PHENYL)-ETHANONE
• Synonyms: 2-Bromo-3',4'-dimethylacetophenone
• CAS NO: 2633-50-3
• Molecular Formula: C₁₀H₁₁BrO
• Molecular Weight: 227.1
• Mol File: 2633-50-3.mol
• Article Data: 9

Chemical Properties

• Melting Point: 65 °C
• Boiling Point: 292.6 °C at 760 mmHg
• Flash Point: 72.4 °C
• Appearance: /
• Density: 1.362 g/cm³
• Vapor Pressure: 0.00182mmHg at 25°C
• Refractive Index: 1.557
• CAS DataBase Reference: 2-BROMO-1-(3,4-DIMETHYL-PHENYL)-ETHANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-1-(3,4-DIMETHYL-PHENYL)-ETHANONE(2633-50-3)
• EPA Substance Registry System: 2-BROMO-1-(3,4-DIMETHYL-PHENYL)-ETHANONE(2633-50-3)

Safety Data

• Hazardous Substances Data: 2633-50-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H11BrO/c1-7-3-4-9(5-8(7)2)10(12)6-11/h3-5H,6H2,1-2H3

Upstream product

• 95-47-6 o-xylene 
• 598-21-0 2-Bromoacetyl bromide 
• 108773-84-8 3-Bromomethyl-3-(3,4-dimethyl-phenyl)-4,4-dimethyl-[1,2]dioxetane 
• 3637-01-2 3,4-dimethylacetophenone 

Downstream Products

• 85018-99-1 1-(3,4-dimethyl-phenacyl)-pyridinium; bromide 
• 385815-40-7 2-(3,4-dimethyl-phenyl)-indolizine 
• 313528-18-6 2-(3,4-dimethylphenyl)imidazo[1,2-a]pyridine 
• 110179-23-2 2-(3,4-dimethyl-phenyl)-imidazo[1,2-a]pyrimidine 
• 6097-19-4 1-(3,4-dimethylphenyl)-2-thiocyanatoethan-1-one 
• 109470-04-4 2-(3,4-dimethyl-phenyl)-5-methoxy-indole 
• 739302-02-4 1-(3,4-dimethyl-phenyl)-2-(2-imino-thiazol-3-yl)-ethanone 
• 103793-35-7 1-Methyl-3-[2-(3,4-dimethylphenyl)-2-oxoethyl]-1H-imidazolium bromide 
• 129972-99-2 N-[2-(3,4-Dimethyl-phenyl)-2-oxo-ethyl]-formamide 
• 129972-95-8 C₁₂H₁₃NO₃ 
• 90874-60-5 ω-Amino-3,4-dimethyl-acetophenon 
• 113813-43-7 Phosphoric acid 1-(3,4-dimethyl-phenyl)-vinyl ester dimethyl ester 
• 113813-45-9 Phosphoric acid 1-(3,4-dimethyl-phenyl)-vinyl ester diethyl ester 
• 20973-21-1 ω-(dibenzylamino)-3,4-dimethylacetophenone 

Relevant articles and documents

Polysubstituted Ligand Framework for Color Tuning Phosphorescent Iridium(III) Complexes

A series of ligands have been synthesized based upon a polysubstituted 2-phenylquinoxaline core structure. These ligands introduce different combinations of fluorine and methyl substituents on both the phenyl and quinoxaline constituent rings. The resultant investigation of these species as cyclometalating agents for Ir(III) gave cationic complexes of the form [Ir(C^N)2(bipy)]PF6 (where C^N = cyclometalating ligand; bipy = 2,2′-bipyridine). X-ray crystallographic studies were conducted on four complexes and each revealed the expected distorted octahedral geometry based upon a cis-C,C and trans-N,N ligand arrangement at Ir(III). Supporting computational studies predict that each of the complexes share the same general descriptions for the frontier orbitals. TD-DFT calculations suggest MLCT contributions to the lowest energy absorption and a likely MLCT/ILCT/LLCT nature to the emitting state. Experimentally, the complexes display tunable luminescence across the yellow-orange-red part of the visible spectrum (λem = 579-655 nm).

SUBSTITUTED DIHYDROPYRAZOLO PYRAZINE CARBOXAMIDE DERIVATIVES

The invention relates to substituted dihydropyrazolo pyrazine carboxamide derivatives and to processes for their preparation, and also to their use for preparing medicaments for the treatment and/or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.

DERIVATIVES OF BENZOTHIAZINES, PREPARATION THEREOF AND APPLICATION THEREOF AS DRUGS

The object of the present invention is benzothiazine derivatives having the capability of inhibiting 11β-HSD1 not only at an enzymatic level but also at a cell level. The compounds of the present invention are of general formula (I). Wherein notably R1 represents a hydrogen or OR1 represents an ester or an ether. R2 represents a naphthyl or a 1, 2, 3, 4-tetrahydro-naphthalene or a biphenyl or phenyl pyridine or a substituted phenyl. R3 represents a methyl or ethyl; R4 and R'4 represent a hydrogen.