1164104-62-4

Basic information

• Product Name: (R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol
• Synonyms: (R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol
• CAS NO: 1164104-62-4
• Molecular Weight: 580.967
• Mol File: 1164104-62-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol(1164104-62-4)
• EPA Substance Registry System: (R,E)-3-(tert-butyldiphenylsilyloxy)-2-(octadec-2-en-1-yloxy)propan-1-ol(1164104-62-4)

Safety Data

• Hazardous Substances Data: 1164104-62-4(Hazardous Substances Data)

Upstream product

• 2831-86-9 trans-octadec-2-en-1-ol 
• 107033-46-5 (R)-(tert-butyldiphenylsilyloxy)methyloxirane 

Relevant articles and documents

Synthesis and antioxidant properties of an unnatural plasmalogen analogue bearing a trans O-vinyl ether linkage

To assess the antioxidant behavior of trans-1, we first synthesized trans-allyl ether 4 by opening an (S)-glycildol derivative with an (E)-alk-2en-ol, and then produced the unnatural E-enol ether 1 by a stereoselective iridium(I)-catalyzed olefin isomerization. Natural cis-1 was preferentially degraded by HOCI and was more protective than trans-1 against lipid peroxidation Induced by a free-radical Initiator, demonstrating that the geometry of the 1-alkenyloxy bond participates In the antioxidant defensive role of 1.