63650-24-8

Basic information

• Product Name: 2-(4-chlorophenoxy)propan-1-ol
• Synonyms: 1-propanol, 2-(4-chlorophenoxy)-; 2-(4-Chlorophenoxy)propan-1-ol
• CAS NO: 63650-24-8
• Molecular Formula: C₉H₁₁ClO₂
• Molecular Weight: 186.6354
• Mol File: 63650-24-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 286.4°C at 760 mmHg
• Flash Point: 127°C
• Density: 1.194g/cm³
• Vapor Pressure: 0.00123mmHg at 25°C
• Refractive Index: 1.534
• CAS DataBase Reference: 2-(4-chlorophenoxy)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chlorophenoxy)propan-1-ol(63650-24-8)
• EPA Substance Registry System: 2-(4-chlorophenoxy)propan-1-ol(63650-24-8)

Safety Data

• Hazardous Substances Data: 63650-24-8(Hazardous Substances Data)

Upstream product

• 3307-39-9 2-(4-chlorophenoxy)propionic acid 
• 18671-89-1 cyclopropyl 4-(2-chlorophenoxy)butanoate 
• 78-89-7 2-chloro-1-propanol 
• 106-48-9 4-chloro-phenol 
• 75-56-9 methyloxirane 
• 4878-20-0 2-(4-Chlorophenoxy)propionic acid chloride 
• 4169-04-4 2-phenoxy-1-propanol 
• 95262-84-3 2-(4-chlorophenoxy)propanoic acid methyl ester 

Downstream Products

• 69183-35-3 {4-[2-(4-Chloro-phenoxy)-propoxy]-phenyl}-acetic acid methyl ester 
• 175442-03-2 2-(4-chlorophenoxy)propionaldehyde 
• 69183-69-3 {4-[2-(4-Chloro-phenoxy)-propoxy]-phenyl}-acetic acid 
• 69183-41-1 (4-Chloro-phenoxy)-{4-[2-(4-chloro-phenoxy)-propoxy]-phenyl}-acetic acid 
• 69183-39-7 (4-tert-Butyl-phenoxy)-{4-[2-(4-chloro-phenoxy)-propoxy]-phenyl}-acetic acid 
• 69183-42-2 {4-[2-(4-Chloro-phenoxy)-propoxy]-phenyl}-(4-trifluoromethyl-phenoxy)-acetic acid 
• 63650-13-5 2-(4-chlorophenoxy)-1-propanol O-methanesulfonate 
• 3307-39-9 2-(4-chlorophenoxy)propionic acid 
• 98919-13-2 2-(2,4-dichlorophenoxy)propan-1-ol 
• 120-36-5 2-(2,4-dichlorophenoxy)propionic acid 
• 82703-23-9 O-[2-(4-chlorophenoxy)propyl]hydroxylamine 

Relevant articles and documents

Cyclohexane-1,3-diketone compound as well as synthesis method and application thereof

The invention provides a cyclohexane-1,3-diketone compound of which the structural formula is shown in the specification, wherein the group R1 in the structural formula I is -CH3, -CH2CH3, -(CH2)2CH3,-CH(CH3)2, -(CH2)3CH3, -CH(CH3)C2H5, -CH2CH(CH3)2 or -C

Highly Enantioselective Hydrogenation of Amides via Dynamic Kinetic Resolution Under Low Pressure and Room Temperature

High-throughput screening and lab-scale optimization were combined to develop the catalytic system trans-RuCl2((S,S)-skewphos)((R,R)-dpen), 2-PrONa, and 2-PrOH. This system hydrogenates functionalized α-phenoxy and related amides at room temperature under 4 atm H2 pressure to give chiral alcohols with up to 99% yield and in greater than 99% enantiomeric excess via dynamic kinetic resolution.

Resolution of 2-aryloxy-1-propanols via lipase-catalyzed enantioselective acylation in organic media

2-Aryloxy-1-propanols, primary alcohols with an oxygen atom at the stereocenter, were resolved with good to high enantioselectivity by acylation with vinyl butanoate mediated by Pseudomonas sp. lipase in di-iso-propyl ether. Potential factors affecting the enantioselectivity of the enzymatic acylation were examined: solvents, acyl donors and temperature. Using this enantioselective acylation procedure, enantiomerically pure (R)-2-(4-chlorophenoxy)-1-propanol was prepared on a gram scale.