1448608-14-7

Basic information

• Product Name: C₁₈H₃₃IO₄Si
• Synonyms: C₁₈H₃₃IO₄Si
• CAS NO: 1448608-14-7
• Molecular Weight: 468.448
• Mol File: 1448608-14-7.mol

Chemical Properties

• CAS DataBase Reference: C₁₈H₃₃IO₄Si(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₃₃IO₄Si(1448608-14-7)
• EPA Substance Registry System: C₁₈H₃₃IO₄Si(1448608-14-7)

Safety Data

• Hazardous Substances Data: 1448608-14-7(Hazardous Substances Data)

Upstream product

• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 
• 165611-18-7 (3aS,4R,5R,7aS)-7-iodo-2,2-dimethyl-3a,4,5,7a-tetrahydro-1,3-benzodioxole-4,5-diol 

Downstream Products

• 1380508-49-5 (1R,2R,3R,4R)-3-methoxy-6-(7-methyl-3-methylene-oct-6-en-1-ynyl)-cyclohex-5-ene-1,2,4-triol 
• 1448608-19-2 1,2,4-O,O′,O″-triacetylphomentrioloxin 

Relevant articles and documents

Chemoenzymatic total synthesis of the phytotoxic geranylcyclohexentriol (-)-phomentrioloxin

The enantiomeric form, 1R, of the structure (1S) assigned to the phytotoxic natural product phomentrioloxin has been synthesized in seven steps from the homochiral cis-1,2-dihydrocatechol 3. These studies reveal that the true structure of phomentrioloxin

The Synthesis of Certain Phomentrioloxin A Analogues and Their Evaluation as Herbicidal Agents

A series of 28 analogues of the phytotoxic geranylcyclohexentriol (-)-phomentrioloxin A (1) has been synthesized through cross-couplings of various enantiomerically pure haloconduritols or certain deoxygenated derivatives with either terminal alkynes or borylated alkenes. Some of these analogues display modest herbicidal activities, and physiological profiling studies suggest that analogue 4 inhibits photosystem II in isolated thylakoids in vitro.