142363-61-9

Basic information

• Product Name: 2-bromo-1-(2-methoxyphenyl)ethan-1-ol
• Synonyms: 2-bromo-1-(2-methoxyphenyl)ethan-1-ol
• CAS NO: 142363-61-9
• Molecular Weight: 231.089
• Mol File: 142363-61-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-bromo-1-(2-methoxyphenyl)ethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-1-(2-methoxyphenyl)ethan-1-ol(142363-61-9)
• EPA Substance Registry System: 2-bromo-1-(2-methoxyphenyl)ethan-1-ol(142363-61-9)

Safety Data

• Hazardous Substances Data: 142363-61-9(Hazardous Substances Data)

Upstream product

• 31949-21-0 bromomethyl 2-methoxyphenyl ketone 

Downstream Products

• 1608496-97-4 C₂₅H₃₀N₂O₅ 
• 1608496-88-3 C₂₀H₂₂N₂O₃ 
• 1613220-25-9 C₂₅H₃₁BrN₂O₅ 
• 142363-71-1 2-(2-methoxyphenyl)-4-n-propylmorpholine 
• 142363-67-5 6-(2-methoxyphenyl)-4-n-propylmorpholin-3-one 
• 142363-63-1 1-(2-methoxyphenyl)-2-(n-propylamino)ethanol 
• 62717-78-6 2-(2-methoxyphenyl)oxirane 

Relevant articles and documents

Lithium triethylborohydride as catalyst for solvent-free hydroboration of aldehydes and ketones

Commercially available and inexpensive lithium triethylborohydride (LiHBEt3) acts as efficient catalyst for the solvent-free hydroboration of a wide range of aldehydes and ketones, which were subsequently transformed to corresponding 1° and 2° alcohols in one-pot procedure at room temperature (rt).

Chiral styrene oxides from α-haloacetophenones using NaBH4 and TarB-NO2, a chiral Lewis acid

High enantioselectivities are obtained for the preparation of chiral styrene oxides through reduction of α-haloacetophenones using TarB-NO 2 reagent and the inexpensive and mild reducing agent NaBH 4. The epoxides are easily obtained in up to 95% ee through routine acid-base workup of the product alcohols. Either the (R) or (S) epoxide can be obtained by using the appropriate l- or d-tartaric acid starting material in the TarB-NO2 reagent.