602277-07-6

Usage

Molecular Structure

A complex molecular structure with a hepten backbone, a phenyl side group, a silyl ether, and a methoxy group attached.

Classification

It is an organosilicon compound and belongs to the class of alcohols.

Functional Groups

It contains an alcohol group (-OH) at the first carbon, a double bond (C=C) at the first and third carbons, a methyl group (-CH3) at the fourth carbon, a methoxy group (-OCH3) at the fifth carbon, and a silyl ether group (-Si) at the sixth carbon.

Substituents

The silyl ether group has a (1,1-dimethylethyl)dimethylsilyl structure.

Potential Uses

The precise chemical properties and potential uses of 1-Hepten-3-ol, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-methoxy-4-methyl-1-phenyl-, (1E,3R,4R,5R)- would depend on its exact structure and how it interacts with other substances.

Importance

It is crucial for researchers and chemists to study and understand the characteristics of 1-Hepten-3-ol, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-5-methoxy-4-methyl-1-phenyl-, (1E,3R,4R,5R)- thoroughly.

Upstream product

• 69739-34-0 t-butyldimethylsiyl triflate 
• 602277-06-5 (E)-(3R,4R,5R)-3-Methoxy-4-methyl-7-phenyl-hept-6-ene-2,5-diol 
• 23397-76-4 1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose 
• 602277-04-3 (3R,4R,5R)-2,3-Dimethoxy-4-methyl-5-((E)-styryl)-tetrahydro-furan 
• 602276-98-2 C₁₉H₂₈O₅ 
• 602276-99-3 C₁₉H₃₀O₅ 
• 602277-02-1 C₁₉H₂₄O₃ 
• 602277-00-9 C₁₃H₂₂O₅ 
• 602277-01-0 C₁₃H₂₀O₃ 
• 602277-03-2 (3R,4S,5R)-2-Methoxy-4-methyl-5-((E)-styryl)-tetrahydro-furan-3-ol 
• 602277-05-4 (3R,4R,5R)-3-Methoxy-4-methyl-5-((E)-styryl)-tetrahydro-furan-2-ol 
• 18546-21-9 1,2:5,6-di-O-cyclohexylidene-α-D-ribo-3-hexofuranose-3-ulose 

Downstream Products

• 307492-71-3 3,5-dimethoxy-2,4-dimethyl-7-phenyl-(2S,3S,4R,5S,6E)-6-hepten-1-ol 
• 602277-11-2 (E)-(3R,4R,5S)-3,5-Dimethoxy-4-methyl-7-phenyl-hept-6-en-2-one 
• 602277-10-1 (E)-(3R,4R,5S)-3,5-Dimethoxy-4-methyl-7-phenyl-hept-6-en-2-ol 
• 602277-12-3 ((E)-(3S,4R,5R)-3,5-Dimethoxy-4,6-dimethyl-hepta-1,6-dienyl)-benzene 
• 602277-09-8 tert-Butyl-((E)-(2R,3R,4S)-2,4-dimethoxy-1,3-dimethyl-6-phenyl-hex-5-enyloxy)-dimethyl-silane 
• 602277-08-7 (E)-(3S,4R,5R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-methoxy-4-methyl-1-phenyl-hept-1-en-3-ol 

Relevant academic research and scientific papers

Carbohydrate-based synthesis of crocacin: Stereoselective Heck reaction of carbohydrate 5,6-ene- and 5,6-yne-derivatives with aromatic halides

The Heck reaction between a carbohydrate 5,6-ene derivative 9 and an aromatic halide exclusively gave rise to the β-carbohydrate-substituted trans-styrene derivative 8; while the corresponding Wittig reaction produced a cis/trans mixture in which the cis-