417698-17-0

Basic information

• Product Name: O-2-trimethylsilylphenyl N-isopropylcarbamate
• Synonyms: O-2-trimethylsilylphenyl N-isopropylcarbamate
• CAS NO: 417698-17-0
• Molecular Weight: 251.401
• Mol File: 417698-17-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: O-2-trimethylsilylphenyl N-isopropylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: O-2-trimethylsilylphenyl N-isopropylcarbamate(417698-17-0)
• EPA Substance Registry System: O-2-trimethylsilylphenyl N-isopropylcarbamate(417698-17-0)

Safety Data

• Hazardous Substances Data: 417698-17-0(Hazardous Substances Data)

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 17614-10-7 phenyl N-isopropylcarbamate 
• 108-95-2 phenol 

Downstream Products

• 15288-53-6 o-(trimethylsilyl)phenol 
• 444095-29-8 2-hydroxy-3-(trimethylsilyl)benzaldehyde 
• 2040-86-0 2-bromo-6-iodophenol 
• 899427-35-1 2-(tert-butyldimethylsilyloxy)phenylmethyl-6-(trimethylsilyl)phenyl isopropylcarbamate 
• 899427-37-3 2-(tert-butyldimethylsilyloxy)phenylmethyl-6-iodophenyl isopropylcarbamate 
• 899427-34-0 acetic acid (2-isopropylcarbamoyloxy-3-trimethylsilanyl-phenyl)-phenyl-methyl ester 
• 899427-31-7 2-hydroxyphenylmethyl-6-(trimethylsilyl)phenyl isopropylcarbamate 
• 899427-30-6 2-benzoyl-6-(trimethylsilyl)phenyl isopropylcarbamate 
• 899427-36-2 acetic acid (3-iodo-2-isopropylcarbamoyloxy-phenyl)-phenyl-methyl ester 
• 899427-33-9 2-benzoyl-6-iodophenyl isopropylcarbamate 
• 899427-38-4 2-hydroxyphenylmethyl-6-iodophenyl isopropylcarbamate 
• 899427-29-3 2-bromo-6-(trimethylsilyl)phenyl isopropylcarbamate 
• 899427-32-8 2-bromo-6-iodophenyl isopropylcarbamate 

Relevant articles and documents

Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate: A versatile precursor to o-benzyne

(Chemical Equation Presented) An efficient procedure for the gram-scale preparation of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate, a versatile precursor to o-benzyne, is presented. The three-step sequence utilizes phenol as the starting material, requires only one chromatographic purification, and ultimately delivers the desired silyltriflate in 66% overall yield. 2009 American Chemical Society.