141694-60-2

Basic information

• Product Name: Benzene, (3,3-diiodopropyl)-
• CAS NO: 141694-60-2
• Molecular Formula: C9H10I2
• Molecular Weight: 371.987
• Mol File: 141694-60-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, (3,3-diiodopropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (3,3-diiodopropyl)-(141694-60-2)
• EPA Substance Registry System: Benzene, (3,3-diiodopropyl)-(141694-60-2)

Safety Data

• Hazardous Substances Data: 141694-60-2(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 10147-11-2 propargyl benzene 
• 141694-57-7 Trifluoro-methanesulfonic acid 3-phenyl-1-trifluoromethanesulfonyloxy-propyl ester 

Downstream Products

• 141694-63-5 (E)-1-iodo-3-phenyl-1-propene 
• 71804-70-1 (Z)-1-iodo-3-phenylpropene 
• 63213-07-0 4-methyl-1-phenylhexane 
• 2049-94-7 (3-methylbutyl)benzene 

Relevant articles and documents

A new approach towards the synthesis of sp3 1,1-diiodoalkanes

An easy and straightforward method for the synthesis of gem-diiodo derivatives is reported.

Carbocupration/zinc carbenoid homologation and β-elimination reactions for a new synthesis of allenes - Application to the enantioselective synthesis of chiral allenes by deracemization of sp3-organometallic derivatives

A new and straightforward carbocupration/zinc homologation/β-elimination reaction sequence allows the one-pot synthesis of polysubstituted allenes from acetylenic sulfoxides in excellent isolated chemical yields. Secondary zinc carbenoids were used for the homologation reaction, and so a new synthesis of 1,1-diiodoalkanes is described. This methodology also allows the synthesis of chiral allenes through thermodynamic equilibration of secondary organometallic derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2002.