72733-58-5

Basic information

• Product Name: Cyclopropanemethanol, 2,2-dichloro-3-phenyl-
• CAS NO: 72733-58-5
• Molecular Formula: C10H10Cl2O
• Molecular Weight: 217.095
• Mol File: 72733-58-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclopropanemethanol, 2,2-dichloro-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopropanemethanol, 2,2-dichloro-3-phenyl-(72733-58-5)
• EPA Substance Registry System: Cyclopropanemethanol, 2,2-dichloro-3-phenyl-(72733-58-5)

Safety Data

• Hazardous Substances Data: 72733-58-5(Hazardous Substances Data)

Upstream product

• 57976-72-4 2,2-dichloro-3-phenyl-cyclopropanecarboxaldehyde 
• 20615-52-5 (E)-(3-(1-ethoxyethoxy)prop-1-en-1-yl)benzene 
• 67-66-3 chloroform 
• 104-54-1 3-Phenylpropenol 

Downstream Products

• 139387-01-2 2-chloro-3-phenylcyclopropanecarboxaldehyde 
• 53646-88-1 1-benzyl-3-phenyl-1H-pyrrole 
• 34266-21-2 1,1-dichloro-t-3-phenylcyclopropane-r-2-carboxylic acid 
• 139387-02-3 (2-Chloro-3-phenyl-cyclopropyl)-methanol 

Relevant articles and documents

Hydroxamic acid and N-hydroxyurea derivatives and their use

Certain novel hydroxamic acid derivatives having the structure inhibit the enzyme lipoxygenase. These compounds, and the pharmaceutically acceptable salts thereof, are useful in the treatment or alleviation of inflammatory diseases, allergic conditions and cardiovascular diseases in mammals and as the active ingredient in pharmaceutical compositions for treating such conditions.

REACTION OF DICHLOROCARBENE WITH ALLYL AND CINNAMYL ALCOHOLS

In the reaction of dichlorocarbene, generated by the phase-transfer method, with allyl and cinnamyl alcohols both the products from addition of the dichlorocarbene to the double bond and the products from substitution of the hydroxyl group by a chlorine atom and simultaneous addition of dichlorocarbene at the double bond are formed.