89968-81-0

Basic information

• Product Name: 1-Phenylpentane-1,4-diol
• CAS NO: 89968-81-0
• Molecular Weight: 180.247
• Mol File: 89968-81-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1-Phenylpentane-1,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenylpentane-1,4-diol(89968-81-0)
• EPA Substance Registry System: 1-Phenylpentane-1,4-diol(89968-81-0)

Safety Data

• Hazardous Substances Data: 89968-81-0(Hazardous Substances Data)

Upstream product

• 127811-25-0 2-Nitro-1-phenyl-pentane-1,4-diol 
• 583-05-1 1-phenylpentane-1,4-dione 
• 36866-66-7 5-phenyloxolan-2-ol 
• 917-54-4 methyllithium 
• 100-52-7 benzaldehyde 
• 861399-10-2 (RS)-1-(n-butyltellanyl)-3-butanol 
• 132205-09-5 (1R*,2Z,4S*)/(1R*,2Z,4R*)-1-Phenyl-2-pentene-1,4-diol 
• 1228681-29-5 1-phenyl-2-pentene-1,4-diol 
• 109-72-8 n-butyllithium 
• 6089-15-2 4-iodo-butan-2-ol 
• 135468-12-1 1-phenylpent-2-yne-1,4-diol 
• 622-42-4 1-nitro-1-phenylmethane 
• 78-94-4 methyl vinyl ketone 
• 27998-52-3 (+/-)-4-(phenylthio)-2-butanol 

Downstream Products

• 3042-21-5 2-methyl-5-phenyl-1H-pyrrole 
• 533883-16-8 1-hexyl-2-phenyl-5-methylpyrrole 
• 154592-40-2 3,4-dihydro-2-methyl-5-phenyl-2H-pyrrole 
• 4457-59-4 tetrahydro-2-methyl-5-phenylfuran 
• 1009-14-9 phenyl butyl ketone 
• 27927-59-9 4-hydroxy-1-phenylpentan-1-one 
• 583-05-1 1-phenylpentane-1,4-dione 

Relevant articles and documents

Nonclassical Mechanism in the Cyclodehydration of Diols Catalyzed by a Bifunctional Iridium Complex

1,4- and 1,5-diols undergo cyclodehydration upon treatment with cationic N-heterocyclic carbene (NHC)–IrIII complexes to give tetrahydrofurans and tetrahydropyrans, respectively. The mechanism was investigated, and a metal-hydride-driven pathway was proposed for all substrates, except for very electron-rich ones. This contrasts with the well-established classical pathways that involve nucleophilic substitution.

Non-flammable and reusable hydrogenation of aromatic ketones in ionic liquid

A novel method of hydrogenation of aromatic ketones in the ionic liquid [BHEA][HCO2] was developed; this method is more enhanced in terms of flammability and reusability as compared to the conventional method (H 2 and Pd/C). The redu

γ-Butyltelluro-2-butanol: A route to reactive 1,4-dianion intermediates

γ-Butyltelluro-2-butanol was reacted with 2 equiv of n-butyllithium. Both tellurium/lithium exchange and the proton abstraction reactions took place in a single step and the lithium dianion intermediate efficiently reacted with aldehydes and ketones, producing the corresponding diols.