143427-44-5

Basic information

• Product Name: Benzenemethanol, a-(2-chloroethyl)-a-2-propenyl-
• Synonyms: 1-Chloro-3-phenyl-hex-5-en-3-ol;1-chloro-3-phenylhex-5-en-3-ol
• CAS NO: 143427-44-5
• Molecular Formula: C12H15ClO
• Molecular Weight: 210.704
• Mol File: 143427-44-5.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 90 °C (0.1 mmHg)
• CAS DataBase Reference: Benzenemethanol, a-(2-chloroethyl)-a-2-propenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-(2-chloroethyl)-a-2-propenyl-(143427-44-5)
• EPA Substance Registry System: Benzenemethanol, a-(2-chloroethyl)-a-2-propenyl-(143427-44-5)

Safety Data

• Hazardous Substances Data: 143427-44-5(Hazardous Substances Data)

Upstream product

• 936-59-4 3-chloropropiophenone 
• 15336-98-8 diallyldibutyltin 
• 54655-41-3 B-allyl-1,3,2-dioxaborinane 
• 7393-43-3 tetraallyl tin 
• 72824-04-5 2-Allyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 106-95-6 allyl bromide 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 1114066-14-6 1-phenethylamino-3-phenyl-hex-5-en-3-ol 
• 1110641-87-6 6-allyl-6-phenyl-3-(2-phenylcyclopropyl)-1,3-oxazinan-2-one 
• 1114084-55-7 (S)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1110642-01-7 (R)-6-allyl-3-((S)-1-(4-bromophenyl)ethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1110642-31-3 (R)-6-allyl-3-((S)-1-(4'-fluoro-[1,1'-biphenyl]-4-yl)ethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1321599-87-4 (R)-6-allyl-3-((S)-1-(4'-fluoro-[1,1'-biphenyl]-4-yl)propyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114085-85-6 (R)-3-((S)-1-(4'-fluorobiphenyl-4-yl)propyl)-6-(3-hydroxypropyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114065-84-7 (R)-3-((S)-1-(4'-fluorobiphenyl-4-yl)ethyl)-6-(3-hydroxypropyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114065-78-9 (S)-3-((S)-1-(4'-fluorobiphenyl-4-yl)ethyl)-6-(2-hydroxyethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114065-94-9 (R)-3-((S)-1-(2',4'-difluorobiphenyl-4-yl)ethyl)-6-(3-hydroxypropyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114065-86-9 (S)-3-((S)-1-(2',4'-difluorobiphenyl-4-yl)ethyl)-6-(2-hydroxyethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1114065-95-0 (R)-6-allyl-3-((S)-1-(2',4'-difluoro-[1,1'-biphenyl]-4-yl)ethyl)-6-phenyl-1,3-oxazinan-2-one 
• 1110641-90-1 (R)-6-allyl-3-((S)-1-(4-bromophenyl)propyl)-6-phenyl-1,3-oxazinan-2-one 
• 1259034-42-8 (S)-3-((S)-1-(4-(4-(azetidin-1-yl)-3,3-dimethyl-4-oxobut-1-ynyl)phenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one 

Relevant articles and documents

Asymmetric allylation of ketones and subsequent tandem reactions catalyzed by a novel polymer-supported titanium-binolate complex

By using a novel, simple, and convenient synthetic route, enantiopure 6-ethynyl-BINOL (BINOL=1,1-binaphthol) was synthesized and anchored to an azidomethylpolystyrene resin through a copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction. The polyst

CYCLIC INHIBITORS OF 11BETA-HYDROXYSTEROID DEHYDROGENASE 1

This invention relates to novel compounds of the Formula (I), (II), (II-A), (Il-B), (ll-C), (ll-D), (III). (III-A). (IIIl-B). (IIl-C). (IIl-D), (III-E) (IV), (IV-A), (IV-B). (IV-C), (IV-D). (V), (V-A), (V-B), (V-C), (V-D), pharmaceutically acceptable salt

Mild and general zinc-alkoxide-catalyzed allylations of ketones with allyl pinacol boronates

A general and efficient zinc-alkoxide-catalyzed allylation of a diverse array of ketones with allyl boronates is presented. The methodology is effective with 2 mol % of catalyst and with relatively short reaction times. Studies of the key exchange process are presented, which support a cyclic transition state for the boron to zinc exchange.