148367-01-5

Basic information

• Product Name: 1-(4-isobutylphenyl)pentan-1-one
• Synonyms: 1-(4-isobutylphenyl)pentan-1-one
• CAS NO: 148367-01-5
• Molecular Weight: 218.339
• Mol File: 148367-01-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(4-isobutylphenyl)pentan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-isobutylphenyl)pentan-1-one(148367-01-5)
• EPA Substance Registry System: 1-(4-isobutylphenyl)pentan-1-one(148367-01-5)

Safety Data

• Hazardous Substances Data: 148367-01-5(Hazardous Substances Data)

Upstream product

• 538-93-2 1-phenyl-2-methylpropane 
• 638-29-9 n-valeryl chloride 

Downstream Products

• 148366-62-5 ethyl 4-[3-[4-[1-(4-isobutylphenyl)pentyloxy]benzoyl]indol-1-yl]butyrate 
• 148366-77-2 4-(3-{4-[(S)-1-(4-Isobutyl-phenyl)-pentyloxy]-benzoyl}-indol-1-yl)-butyric acid ethyl ester 
• 148366-78-3 4-(3-{4-[(R)-1-(4-Isobutyl-phenyl)-pentyloxy]-benzoyl}-indol-1-yl)-butyric acid ethyl ester 
• 146939-45-9 ethyl 4-[1-[4-[1-(4-isobutylphenyl)pentyloxy]benzoyl]indolizin-3-yl]butyrate 
• 148367-08-2 1-bromo-1-(4-isobutylphenyl)pentane 
• 148367-04-8 1-(4-Isobutylphenyl)pentan-1-ol 
• 148367-12-8 (S)-1-(4-Isobutyl-phenyl)-pentan-1-ol 
• 148367-11-7 (R)-1-(4-Isobutyl-phenyl)-pentan-1-ol 

Relevant articles and documents

A 4 - isobutyl phenyl ketone compounds (by machine translation)

The invention discloses a 4 - isobutyl phenyl ketone compounds, the compound structure is as follows: said compound 4 - isobutyl-benzene as the starting material, substituted sulfonic acid and substituted sulfonate as the catalyst, the reaction with the acyl chloride, the following reaction: the application of this method to synthesize 4 - isobutyl phenyl ketone compound, simple and convenient operation, mild reaction conditions, environment-friendly, and has excellent industrial prospect. (by machine translation)

Indole derivatives useful as testosterone 5α-reductase inhibitors

A compound of the formula (I): STR1 wherein R 1 is an optionally protected carboxy(lower)alkyl, R 2 is a hydrogen, an optionally substituted aryl or a carboxy,X is a bond, --0--, --NH-- or a cycloalkylene, andY is an alkylene which may be interrupted by an oxygen atom, an alkenylene or an alkadienylene,or a pharmaceutically acceptable salt thereof. The compound of the present invention is useful as a testosterone 5α-reductase inhibitor and effective against testosterone 5α-reductase-mediated diseases such as prostatism, prostatic hypertrophy, prostatic cancer, alopecia, hirsutism (e.g. female hirsutism), androgenic alopecia (or male-pattern baldness), acne (e.g. acne vulgaris, pimple), and other hyperandrogenisms.