33602-15-2

Basic information

• Product Name: bornyl chloride
• Synonyms: bornyl chloride
• CAS NO: 33602-15-2
• Molecular Weight: 172.698
• Mol File: 33602-15-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: bornyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: bornyl chloride(33602-15-2)
• EPA Substance Registry System: bornyl chloride(33602-15-2)

Safety Data

• Hazardous Substances Data: 33602-15-2(Hazardous Substances Data)

Upstream product

• 4443-51-0 exo-2-Methoxy-1,7,7-trimethylbicyclo[2.2.1]heptane 
• 565-00-4 dl-camphene 
• 80-56-8 rac-α-pinene 
• 465-30-5 3-chloro-2.2.3-trimethyl-norbornane of uncertain configuration 
• 98-95-3 nitrobenzene 
• 75-36-5 acetyl chloride 
• 62-53-3 aniline 
• 71-43-2 benzene 
• 177698-19-0 Beta-pinene 
• 7782-50-5 chlorine 
• 7446-70-0 aluminium trichloride 
• 60-29-7 diethyl ether 
• 79-92-5 camphene 
• 4795-86-2 (1R)-(+)-cis-pinane 

Downstream Products

• 464-41-5 2-endo-chloro-bornane 
• 76-49-3 isobornyl acetate 
• 13429-40-8 camphene hydrate 
• 565-00-4 dl-camphene 
• 79-92-5 camphene 
• 464-78-8 ketopinic acid 
• 6627-72-1 rac-endo-borneol 
• 24393-70-2 isoborneol 
• 3294-52-8 1,7,7,1',7',7'-Hexamethyl-[2,2']binorbornyl 
• 770676-15-8 bornane-2-sulfinic acid 
• 861075-70-9 1,7,7-trimethyl-2-phenyl-norbornane 
• 507-70-0 1,7,7-trimethyl bicyclo[2.2.1]heptan-2-ol 
• 464-17-5 (+-)-bornylene 
• 4443-51-0 exo-2-Methoxy-1,7,7-trimethylbicyclo[2.2.1]heptane 

Relevant articles and documents

A remarkably efficient Markovnikov hydrochlorination of olefins and transformation of nitriles into imidates by use of AcCl and an alcohol

HCl generated by mixing AcCl with EtOH brings about Markovnikov hydrochlorination of olefins in excellent yields. The products are isolated in states of high purity simply by removal of the volatile components under reduced pressure. Further, nitriles are transformed into imidate hydrochlorides on similar treatment with AcCl and an alcohol. This procedure for nitrile-imidate transformation is much more efficient than that used previously, which involved continuous passing of HCl gas into the solution of a nitrile in a solvent such as Et2O or benzene and an alcohol until one equivalent had been absorbed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.