102568-21-8

Basic information

• Product Name: 7-broMo-3,3-diMethyl-3,4-dihydronaphthalen-1(2H)-one
• Synonyms: 7-broMo-3,3-diMethyl-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 102568-21-8
• Molecular Formula: C₁₂H₁₃BrO
• Molecular Weight: 253.13502
• Mol File: 102568-21-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 316.0±31.0 °C(Predicted)
• Appearance: /
• Density: 1.351±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 7-broMo-3,3-diMethyl-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-broMo-3,3-diMethyl-3,4-dihydronaphthalen-1(2H)-one(102568-21-8)
• EPA Substance Registry System: 7-broMo-3,3-diMethyl-3,4-dihydronaphthalen-1(2H)-one(102568-21-8)

Safety Data

• Hazardous Substances Data: 102568-21-8(Hazardous Substances Data)

Upstream product

• 1070-83-3 tert-Butylacetic acid 
• 589-87-7 1,4-bromoiodobenzene 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 102568-18-3 diethyl <2-(4-bromophenyl)-1,1-dimethylethyl>malonate 
• 102568-19-4 <2-(4-bromophenyl)-1,1-dimethylethyl>malonic acid 
• 6802-75-1 diethyl isopropylidenemalonate 
• 102568-20-7 4-(4-bromophenyl)-3,3-dimethylbutanoic acid 

Downstream Products

• 1338091-99-8 3-(2-amino-1,2′,2′-trimethyl-5-oxo-1,5-dihydrospiro[imidazole-4,4′-thiochroman]-6′-yl)benzonitrile 
• 1338091-96-5 2-amino-7′-(3-chloro-5-fluorophenyl)-1,3′,3′-trimethyl-3′,4′-dihydro-2′H-spiro[imidazole-4,1′-naphthalen]-5(1H)-one 
• 1338094-82-8 (E)-N-(7-bromo-3,3-dimethyl-3,4-dihydronaphthalen-1(2H)-ylidene)-1-phenylethanamine 
• 102568-33-2 trans-1-(benzoylamino)-7-cyano-3,3-dimethyl-1,2,3,4-tetrahydro-2-naphthol 

Relevant articles and documents

Ligand-Enabled PdII-Catalyzed Iterative γ-C(sp3)?H Arylation of Free Aliphatic Acid

C?H functionalization of aliphatic carboxylic acids without attaching exogenous auxiliary has been so far limited at the proximal β-position. In this work, we demonstrate a ligand enabled palladium catalyzed first regioselective distal γ-C(sp3)?H function

Synthesis and Antihypertensive Activity of Pyran Oxygen and Amide Nitrogen Replacement Analogues of the Potassium Channel Activator Cromakalim

The synthesis and oral antihypertensive activity in conscious spontaneously hypertensive rats of two new series of compounds related to the prototype potassium channel activator cromakalim (1) are described.In the first series, replacement of the benzopyr