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Structure of 41828-13-1
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This bench-stable aldehyde features a fused bicyclic framework that enhances its reactivity in nucleophilic additions. The carbonyl group at the 1-position enables direct incorporation into complex scaffolds, while the saturated ring system imparts favorable solubility and handling properties for synthetic applications.
5,6,7,8-Tetrahydronaphthalene-1-carbaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biologically relevant scaffolds. Its aldehyde functionality facilitates standard transformations including reductive amination, Grignard additions, and Wittig reactions. The rigid tetralin core provides excellent structural definition for medicinal chemistry applications, while the bench-stable aldehyde group offers predictable reactivity with high functional group tolerance.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: