29528-33-4

Basic information

• Product Name: 4-(pentan-3-yl)phenol
• CAS NO: 29528-33-4
• Molecular Formula: C₁₁H₁₆O
• Molecular Weight: 164.2441
• Mol File: 29528-33-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 247°C at 760 mmHg
• Flash Point: 119.1°C
• Density: 0.96g/cm³
• Vapor Pressure: 0.0167mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: 4-(pentan-3-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(pentan-3-yl)phenol(29528-33-4)
• EPA Substance Registry System: 4-(pentan-3-yl)phenol(29528-33-4)

Safety Data

• Hazardous Substances Data: 29528-33-4(Hazardous Substances Data)

Upstream product

• 96-22-0 pentan-3-one 
• 108-95-2 phenol 
• 7647-01-0 hydrogenchloride 
• 17138-75-9 3-(4'-methoxyphenyl)pentan-3-ol 
• 93-55-0 1-phenyl-propan-1-one 
• 100-07-2 4-methoxy-benzoyl chloride 
• 584-02-1 2-pentanol 
• 6032-29-7 (+/-)-2-pentanol 
• 408318-32-1 3-(4-methoxyphenyl)pent-1-yn-3-ol 
• 408309-63-7 4-(1-ethynyl-ξ-propenyl)-anisole 
• 3600-64-4 3,3-bis(4-hydroxyphenyl)pentane 
• 7446-70-0 aluminium trichloride 
• 616-24-0 3-aminopentane 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 

Downstream Products

• 206262-50-2 2-[4-(1-ethyl-propyl)-phenoxy]-benzenesulfonyl chloride 
• 657429-16-8 2-[4-(1-ethyl-propyl)-phenoxy]-phenylamine 
• 94-06-4 2-(4-Hydroxyphenyl)pentane 
• 17508-94-0 3-<4-Hydroxy-3.5-dinitro-phenyl>-pentan 
• 95021-58-2 1-(1-ethyl-propyl)-4-(3,5-dinitro-benzoyloxy)-benzene 

Relevant articles and documents

COMPOUNDS FOR INHIBITING KSP KINESIN ACTIVITY

The present invention provides compounds of Formula (I) (wherein R1, R3, X, W, Z and ring Y are as defined herein). The present invention also provides compositions comprising these compounds that are useful for treating cellular proliferative diseases or disorders associated with KSP kinesin activity and for inhibiting KSP kinesin activity.

Al3+-exchanged montmorillonite as an effective solid catalyst for selective synthesis of alkylphenols and bisphenols

Al3+-Exchanged montmorillonite-catalyzed aromatic alkylation of phenol with aldehydes produces the corresponding bisphenols mainly or almost solely in good yields, while that with ketones affords selectively the corresponding alkylphenols in mo

Nucleophilic Displacement with Heterocycles as Leaving Groups. Part 16. Reactions of Secondary Alkyl Primary Amines with 5,6,8,9-Tetrahydro-7-phenyldibenzoxanthylium Trifluoromethanesulphonate to give Intermediates Solvolysing without Rearrangement

Representative secondary alkyl primary amines R1R2CHNH2 react with the title pyrylium cation in acetic acid, alcohols, phenols, and NN-dimethylaniline acting as nucleophilic solvents to give O- and C-(secondary alkyl) products.Absence of carbenium ion rearrangements is consistent with reaction via intimate ion-molecule pairs formed rapidly from the corresponding pyridinium cations.