70201-54-6

Basic information

• Product Name: CHEMBRDG-BB 6132253
• Synonyms: CHEMBRDG-BB 6132253;1-(2-Isopropoxyphenyl)ethanone;1-(2-isopropoxyphenyl)ethanone(SALTDATA: FREE)
• CAS NO: 70201-54-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 178.23
• Mol File: 70201-54-6.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 258.3°C at 760 mmHg
• Flash Point: 102.6°C
• Appearance: /
• Density: 0.999g/cm³
• Vapor Pressure: 0.0138mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: CHEMBRDG-BB 6132253(CAS DataBase Reference)
• NIST Chemistry Reference: CHEMBRDG-BB 6132253(70201-54-6)
• EPA Substance Registry System: CHEMBRDG-BB 6132253(70201-54-6)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 70201-54-6(Hazardous Substances Data)

Usage

General Description

CHEMBRDG-BB 6132253 is a chemical compound with the molecular formula C19H20N4O4S. It is a synthetic organic compound that belongs to the class of benzene and substituted derivatives. CHEMBRDG-BB 6132253 has potential biological activity and is commonly used in the pharmaceutical industry as a building block or intermediate for the synthesis of various drugs and pharmaceutical products. Its specific properties and uses may vary depending on the specific application and formulation in which it is used. However, due to its complex structure and potential reactivity, it must be handled and used with proper chemical safety precautions and knowledge.

InChI:InChI=1/C11H14O2/c1-8(2)13-11-7-5-4-6-10(11)9(3)12/h4-8H,1-3H3

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 75-26-3 isopropyl bromide 
• 137556-77-5 2-(2-Acetylphenoxy)-2-methylpropanoic acid 
• 75-30-9 2-iodo-propane 

Downstream Products

• 888-12-0 (E)-2'-hydroxy-chalcone 
• 1449275-05-1 2-bromo-1-(2-isopropoxyphenyl)ethan-1-one 
• 34000-31-2 2',4-dihydroxychalcone 
• 114590-69-1 5,7-dihydroxy-2'-isopropyloxyneoflavone 
• 114590-62-4 2',5,7-trihydroxyneoflavone 
• 937783-03-4 3-[2-(3-benzyloxy-4-methoxyphenyl)oxazol-4-yl]-1-(2-isopropoxyphenyl)propan-1-one 
• 70201-60-4 2'-isopropoxyacetophenone tosylhydrazone 
• 154735-85-0 1-{2-[2-(triethoxysilyl)ethyl]phenyl}ethanone 
• 114590-66-8 2-isopropyloxybenzoylacetic acid ethyl ester 
• 1521-94-4 1,3,3-Trimethyl-1,3-dihydro-1-isobenzofuranol 
• 137556-67-3 2,2,3-Trimethyl-2,3-dihydro-3-benzofuranol 
• 1414813-88-9 1,3-bis(2-isopropoxyphenyl)propane-1,3-dione 
• 1414813-89-0 3,5-bis(2-isopropoxyphenyl)-1H-pyrazole 
• 1414813-90-3 bis(3,5-bis(2-isopropoxyphenyl)-1H-pyrazol-1-yl)methane 

Relevant articles and documents

5-MEMBERED HETEROARYLAMINOSULFONAMIDES FOR TREATING CONDITIONS MEDIATED BY DEFICIENT CFTR ACTIVITY

The invention relates to heteroaryl compounds, pharmaceutically acceptable salts thereof, and pharmaceutical preparations thereof. Also described herein are compositions and the use of such compounds in methods of treating diseases and conditions mediated by deficient CFTR activity, in particular cystic fibrosis.

Achieving Site Selectivity in Metal-Catalyzed Electron-Rich Carbene Transfer Reactions from N-Tosylhydrazones

Catalyst control of the site-selectivity of electron-rich alkyl, aryl disubstituted carbenes generated in situ from o-alkenyl-substituted N-tosylhydrazones was achieved in this study. Exposure of these substrates to copper iodide triggered the formation of α-alkoxy 2H-naphthalenones. This investigation established that changing the catalyst to a rhodium(II) carboxylate turned off cyclization and migration of the electron-rich metal carbene with the β-carboxylate and turned on allylic C-H bond functionalization to diastereoselectively afford 1H-indenes. Examination of the scope of this reaction revealed that ethereal, aminomethylene, and unactivated 2° C-H bonds could be functionalized.

AROMATIC HETEROCYCLIC COMPOUND

The compound represented by the general formula: wherein ring A is benzene which may be substituted and the like; ring B is benzene which may be substituted and the like; X is a single bond and the like; Y is alkyl which may be substituted and the like; Z is CR1 or nitrogen atom; R1 is hydrogen and the like; R2 is alkyl which may be substituted and the like or a pharmaceutically acceptable salt thereof is useful as a prevention/treatment agent of obesity, diabetes, and the like.