51675-53-7

Basic information

• Product Name: (cyclopropylmethyl)(trimethyl)stannane
• Synonyms: Stannane, (cyclopropylmethyl)trimethyl-
• CAS NO: 51675-53-7
• Molecular Formula: C₇H₁₆Sn
• Molecular Weight: 218.9119
• Mol File: 51675-53-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 163.8°C at 760 mmHg
• Flash Point: 47.1°C
• Vapor Pressure: 2.66mmHg at 25°C
• CAS DataBase Reference: (cyclopropylmethyl)(trimethyl)stannane(CAS DataBase Reference)
• NIST Chemistry Reference: (cyclopropylmethyl)(trimethyl)stannane(51675-53-7)
• EPA Substance Registry System: (cyclopropylmethyl)(trimethyl)stannane(51675-53-7)

Safety Data

• Hazardous Substances Data: 51675-53-7(Hazardous Substances Data)

Upstream product

• 33574-02-6 cyclopropylmethyl iodide 
• 17946-71-3 lithium trimethylstannyl 
• 16643-09-7 trimethylstannyl sodium 
• 38423-82-4 potassium trimethylstannate 

Downstream Products

• 106-98-9 1-butylene 
• 7766-51-0 4-iodobut-1-ene 

Relevant articles and documents

Reactions of Cyclopropylcarbinyl Halides with (Trimethylstannyl)alkalis.Evidence That Kinetically Free Intermediates Need Not Be Involved in Cyclopropylcarbinyl to 3-Butenyl Rearrangements

Studies on the reactions of cyclopropylcarbinyl bromide and iodide with trimethylstannyl anionoids have been made with emphasis on counterion, solvent, and addend (tert-butylamine and dicyclohexylphosphine) effects.Both halides yield cyclopropylcarbinyl- and 3-butenyltrimethylstannanes as major products.Depending upon reaction parameters much or all of the latter is shown to be formed by a mechanism or mechanisms which do not involve kinetically free radical or ionic intermediates.With cyclopropylcarbinyl bromide no electron transfer (ET) (free radical) component isobserved in THF or in THF containing 18-crown-6.However, in 20 percent THF- 80 percent benzene a small extent of the ET mechanism is observed in the presence of DCPH.The iodide reacts in THF via SN2 (or equivalent) and halogen-metal exchange (HME) mechanisms leading to the formation of both methylcyclopropane and 1-butene in the presence of traps, indicating that the cyclopropylcarbinyl anion can undergo rearrangement to the 3-butenyl anion in competition with other processes.In the presence of 18-crown-6 and DCPH a small ET component is observed with the iodide.