62085-80-7

Basic information

• Product Name: 2-benzyl-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• Synonyms: 2-benzyl-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
• CAS NO: 62085-80-7
• Molecular Weight: 266.34
• Mol File: 62085-80-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-benzyl-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(62085-80-7)
• EPA Substance Registry System: 2-benzyl-6-methoxy-3,4-dihydronaphthalen-1(2H)-one(62085-80-7)

Safety Data

• Hazardous Substances Data: 62085-80-7(Hazardous Substances Data)

Upstream product

• 50558-94-6 (E)-2-benzylidene-6-methoxy-3,4-dihydronaphthalen-1(2H)-one 
• 100-51-6 benzyl alcohol 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 

Downstream Products

• 1255327-07-1 2-benzyl-6-methoxy-1-trimethylsilyloxytetral-1-ene 
• 1417443-12-9 2-benzyl-2-(difluoromethyl)-6-methoxy-3,4-dihydronaphthalen-1(2H)-one 
• 1314305-78-6 2-benzyl-6-methoxy-1-(trifluoroacetoxy)tetral-1-ene 
• 72861-94-0 2-Benzyl-6-hydroxy-3,4-dihydro-2H-naphthalen-1-one 
• 87384-04-1 2-benzyl-6-methoxy-1-tetralol 
• 77642-76-3 1,2-trans-1-(p-(β-pyrrolidinoethoxy)phenyl)-2-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-71-8 1,2-trans-1-(p-acetoxyphenyl)-2-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-64-9 1-(o-hydroxyphenyl)-2-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 77642-67-2 1-(p-hydroxyphenyl)-2-benzyl-6-methoxy-1,2,3,4-tetrahydronaphthalene 
• 82525-00-6 4-(2-Benzyl-6-methoxy-3,4-dihydro-naphthalen-1-yl)-phenol 

Relevant articles and documents

Asymmetric Transfer Hydrogenation of Arylidene-Substituted Chromanones and Tetralones Catalyzed by Noyori-Ikariya Ru(II) Complexes: One-Pot Reduction of C═C and C═O bonds

3-Arylidenechroman-4-ones and 2-arylidene-1-tetralones are hydrogenated to cis-benzylic alcohols in dr's and er's up to 99:1 via a C═C and C═O one-pot reduction in the presence of 2-5 mol % Noyori-Ikariya-type RuII chiral complexes and HCO2Na as a hydroge

Organocatalyzed enantioselective protonation of silyl enol ethers: Scope, limitations, and application to the preparation of enantioenriched homoisoflavones

In the present work, enantioselective protonation of silyl enol ethers is reported by means of a variety of chiral nitrogen bases as catalysts, mainly derived from cinchona alkaloids, in the presence of various protic nucleophiles as proton source. A detailed study of the most relevant reaction parameters is disclosed allowing high enantioselectivities of up to 92% ee with excellent yields to be achieved under mild and eco-friendly conditions. The synthetic utility of this organocatalytic protonation was demonstrated during the preparation of two homoisoflavones 4a and 4b, isolated from Chlorophytum Inornatum and Scilla Nervosa, which were obtained with 81% and 78% ee, respectively.

Tetrahydronaphthalene and tetrahydroquinoline compounds, their preparation and their use as leukotriene B4(LTB4) antagonists

This invention relates to novel benzopyran and other benzo-fused leukotriene B4 (LTB4) antagonists and the pharmaceutically acceptable salts thereof, to pharmaceutical compositions containing such compounds or a pharmaceutically acceptable salt thereof, and to methods of using such compounds as LTB4 antagonists. The compounds and the pharmaceutically acceptable salts of this invention inhibit the action of LTB4 and are therefore useful in the treatment of LTB4 induced illnesses such as inflammatory disorders including rheumatoid arthritis, osteoarthritis, inflammatory bowel disease, psoriasis and other skin disorders such as eczema, erythema, pruritus and acne, stroke and other forms of reperfusion injury, graft rejection, autoimmune diseases, asthma, and other conditions where marked neutrophil infiltration occurs.