186641-79-2

Basic information

• Product Name: (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal
• Synonyms: (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal
• CAS NO: 186641-79-2
• Molecular Formula: C₂₁H₂₈O₂Si
• Molecular Weight: 340.53132
• Mol File: 186641-79-2.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal(CAS DataBase Reference)
• NIST Chemistry Reference: (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal(186641-79-2)
• EPA Substance Registry System: (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal(186641-79-2)

Safety Data

• Hazardous Substances Data: 186641-79-2(Hazardous Substances Data)

Usage

Description

(3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is an organosilicon compound that is a derivative of butanal. It features a silanol group protected by a tert-butyldiphenylsilyl group, which contributes to its unique structure and functional groups. (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is highly valued in synthetic chemistry due to its versatility and the mild conditions required for selective removal of its protecting group.

Uses

Used in Organic Synthesis:
(3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is used as a building block in organic synthesis for constructing more complex molecules. Its specific properties and functional groups make it a valuable reagent for creating organic molecules with tailored characteristics and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with improved therapeutic properties.
Used in Chemical Research:
(3R)-3-Methyl-4-(tert-buty)diphenylsilyloxy)butanal serves as a versatile tool in chemical research, particularly in the study of organosilicon compounds and their applications. Its selective removal of the tert-butyldiphenylsilyl group under mild conditions makes it an ideal candidate for exploring new synthetic pathways and methodologies.

Upstream product

• 144693-95-8 (4R)-5-(tert-butyldiphenylsilyloxy)-4-methyl-1-pentene 
• 2938-98-9 (R)-2-methylbutane-1,4-diol 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 3641-51-8 2-(R)-methylsuccinic acid 
• 92817-88-4 (2S)-3-{[tert-butyl(diphenyl)silyl]oxy}-2-methylpropanal 
• 138499-16-8 2-[(tert-butyldiphenylsilyl)oxy]ethanol 
• 115869-43-7 (tert-butyldiphenylsilanyloxy)acetaldehyde 
• 917590-73-9 (E)-4-(tert-butyl-diphenyl-silanyloxy)-but-2-enethioic acid S-ethyl ester 
• 917590-87-5 (R)-4-(tert-butyl-diphenyl-silanyloxy)-3-methyl-thiobutyric acid S-ethyl ester 
• 339533-81-2 tert-Butyl-((E)-(R)-4-methoxy-2-methyl-but-3-enyloxy)-diphenyl-silane 
• 154912-70-6 (3R)-4-{[tert-butyl(diphenyl)silyl]oxy}-3-methylbutan-1-ol 
• 186641-76-9 (2R)-1-(tert-butyldiphenylsilyloxy)-3-cyano-2-methylpropane 
• 132117-93-2 (R)-4-[(tert-butyldiphenylsilyl)oxy]-3-methylbut-1-ene 
• 143088-61-3 (2S)-1-bromo-3-[(tert-butyldiphenylsilyl)oxy]-2-methylpropane 

Downstream Products

• 350246-34-3 (2R,4E)-1-(tert-Butyldiphenylsiloxy)-2,5-dimethyl-4-octen-6-one 
• 930120-92-6 (+)-(E)-(R)-6-(tert-butyl-diphenyl-silanyloxy)-5-methyl-hex-2-enethioic acid S-ethyl ester 
• 1619930-74-3 C₂₈H₃₆O₅ 
• 1619930-75-4 C₂₇H₃₆O₆ 
• 1619930-73-2 C₂₇H₃₈O₆ 
• 1619930-71-0 C₄₃H₅₆O₆Si 
• 1619930-72-1 C₂₇H₄₀O₄Si 
• 1619930-70-9 C₃₄H₄₆O₄Si 
• 1598413-55-8 (4S,6R)-7-(tert-butyldiphenylsilyloxy)-6-methylhept-1-en-4-ol 
• 1598413-61-6 tert-butyl-((2S,4S,6R)-2-(2-(4-methoxybenzyloxy)ethyl)-6-((R)-2-methylbut-3-enyl)tetrahydro-2H-pyran-4-yloxy)dimethylsilane 
• 1598413-60-5 (R)-3-((2R,4S,6S)-4-(tert-butyldimethylsilyloxy)-6-(2-(4-methoxybenzyloxy)ethyl)tetrahydro-2H-pyran-2-yl)-2-methylpropan-1-ol 
• 1598413-59-2 tert-butyl-((R)-3-((2R,4S,6S)-4-(tert-butyldimethylsilyloxy)-6-(2-(4-methoxybenzyloxy)ethyl)tetrahydro-2H-pyran-2-yl)-2-methylpropoxy)diphenylsilane 
• 1598413-57-0 (2R,4S,6S)-2-((R)-3-(tert-butyldiphenylsilyloxy)-2-methylpropyl)-6-(2-(4-methoxybenzyloxy)ethyl)tetrahydro-2H-pyran-4-ol 
• 1598413-56-9 (4S,6R)-7-(tert-butyldiphenylsilyloxy)-6-methylhept-1-en-4-yl 3-(4-methoxybenzyloxy) propanoate 

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