52899-63-5

Basic information

• Product Name: Benzonitrile, 5-butyl-2-hydroxy-
• CAS NO: 52899-63-5
• Molecular Formula: C11H13NO
• Molecular Weight: 175.23
• Mol File: 52899-63-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 5-butyl-2-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 5-butyl-2-hydroxy-(52899-63-5)
• EPA Substance Registry System: Benzonitrile, 5-butyl-2-hydroxy-(52899-63-5)

Safety Data

• Hazardous Substances Data: 52899-63-5(Hazardous Substances Data)

Upstream product

• 1638-22-8 4-n-butylphenol 
• 5470-11-1 hydroxylamine hydrochloride 
• 77635-19-9 2-hydroxy-5-n-butylbenzaldehyde 
• 122-56-5 tributyl borane 
• 40530-18-5 5-bromo-2-hydroxybenzonitrile 
• 74317-78-5 2-bromo 4-butylphenol 
• 3180-09-4 ortho-butylphenol 
• 52899-61-3 2-bromo-4-butylphenyl acetate 
• 4160-51-4 1-(4-methoxyphenyl)-1-butanone 
• 78626-43-4 2-bromo-4-n-butylanisole 
• 18272-84-9 4-n-butylanisole 
• 78626-41-2 2-cyano-4-n-butylanisole 
• 52899-62-4 2-cyano 4-butyl phenylacetate 

Downstream Products

• 87260-25-1 4-(4-Propyl-cyclohexyl)-benzoic acid 4-butyl-2-cyano-phenyl ester 
• 65195-02-0 4-n-pentylbiphenyl-(4')-carboxylic acid (2-cyano-4-n-butylphenyl) ester 

Relevant articles and documents

Facile one-pot transformation of phenols into o-cyanophenols

The treatment of phenols with paraformaldehyde in the presence of MgCl2 and Et3N in THF at 80 C, followed by reaction with molecular iodine and aq. ammonia at room temperature provided the corresponding o-cyanophenols in moderate to good yields. The present reaction is a one-pot transformation of phenols into o-cyanophenols using much less expensive reagents than are typically used; the reaction is free of both transition-metals and cyanide. The utility of this reaction was highlighted during our preparation of Febuxostat from p-bromophenol.

Direct B-alkyl Suzuki-Miyaura cross-coupling of trialkyl-boranes with aryl bromides in the presence of unmasked acidic or basic functions and base-labile protections under mild non-aqueous conditions

An efficient and chemoselective palladium-catalyzed direct B-alkyl Suzuki-Miyaura cross-coupling of trialkylboranes with diversely functionalized aryl bromides is described. A wide variety of unmasked acidic or basic functions are tolerated. The mild non-

(2'-Cyano-4'-n-alkyl)phenyl-3-chloro-4-n-alkoxy benzoates and liquid crystal compositions thereof

A new ester compound suitable for use in a liquid crystal composition is provided. The compound is a (2'-cyano-4'-alkyl)phenyl-3-chloro-4 alkoxybenzoate represented by the following formula: STR1 wherein R and R' are selected from straight-chain alkyl gro