1352708-09-8

Basic information

• Product Name: trimethyl((5-methyl-2-phenyl-1,3,2-dioxaborinan-5-yl)methoxy)silane
• Synonyms: trimethyl((5-methyl-2-phenyl-1,3,2-dioxaborinan-5-yl)methoxy)silane
• CAS NO: 1352708-09-8
• Molecular Weight: 278.231
• Mol File: 1352708-09-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: trimethyl((5-methyl-2-phenyl-1,3,2-dioxaborinan-5-yl)methoxy)silane(CAS DataBase Reference)
• NIST Chemistry Reference: trimethyl((5-methyl-2-phenyl-1,3,2-dioxaborinan-5-yl)methoxy)silane(1352708-09-8)
• EPA Substance Registry System: trimethyl((5-methyl-2-phenyl-1,3,2-dioxaborinan-5-yl)methoxy)silane(1352708-09-8)

Safety Data

• Hazardous Substances Data: 1352708-09-8(Hazardous Substances Data)

Upstream product

• 77-85-0 2-(hydroxymethyl)-2-methylpropane-1,3-diol 
• 98-80-6 phenylboronic acid 
• 75-77-4 chloro-trimethyl-silane 
• 52205-01-3 (5-methyl-2-phenyl-[1,3,2]dioxaborinan-5-yl)-methanol 

Downstream Products

• 1372400-45-7 C₂₀H₁₈O₆ 
• 20795-53-3 3-phenylcyclohexanone 
• 1266101-50-1 5-((4-methoxyphenyl)(phenyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 732250-35-0 (R)-4-(phenyl)-3,4-dihydrocoumarin 
• 1372400-65-1 (R)-5-((2-(benzyloxy)phenyl)(phenyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dion 
• 1352708-16-7 (R)-5-((2-(benzyloxy)phenyl)(phenyl)methyl)-2,2-dimethyl-1,3-dioxane-4,6-dion 
• 64145-51-3 3-phenylcyclopentanone 
• 61198-49-0 4-phenyltetrahydropyran-2-one 
• 74395-08-7 3-phenylcycloheptanone 
• 1008-89-5 2-phenylpyridine 

Relevant articles and documents

Stereoselective synthesis of short benzyl malonyl peptides

A Rh-catalyzed addition reaction on non symmetric dehydro alanine retro-peptides is the key step in the reported three-step strategy for the diastereoselective synthesis of differently functionalized benzyl malonyl peptides (74% overall yield).

Rhodium-catalysed enantioselective synthesis of 4-arylchroman-2-ones

The rhodium-catalysed enantioselective 1,4-addition of organoboron reagents to arylidene Meldrum's acids as acceptors, allows convenient access to 4-arylchroman-2-ones with good to excellent levels of enantioselectivity. The use of silyl-protected dioxabo