154627-62-0

Basic information

• Product Name: 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carbaldehyde
• Synonyms: 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carbaldehyde
• CAS NO: 154627-62-0
• Molecular Weight: 307.346
• Mol File: 154627-62-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carbaldehyde(154627-62-0)
• EPA Substance Registry System: 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carbaldehyde(154627-62-0)

Safety Data

• Hazardous Substances Data: 154627-62-0(Hazardous Substances Data)

Upstream product

• 154627-61-9 5-tert-butoxycarbonylamino-5-hydroxymethyl-2-phenyl-1,3-dioxane 
• 24424-99-5 di-tert-butyl dicarbonate 
• 51430-71-8 2-phenyl-5-(hydroxymethyl)-5-nitro-1,3-dioxane 
• 146651-71-0 N-(tert-butyloxycarbonyl)-2-amino-2-(hydroxymethyl)propane-1,3-diol 

Downstream Products

• 154627-63-1 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carboxylic acid 
• 154627-60-8 pentafluorophenyl 5-tert-butoxycarbonylamino-2-phenyl-1,3-dioxane-5-carboxylate 
• 145022-69-1 C₄₉H₇₁N₉O₁₅ 
• 1290540-92-9 C₁₇H₂₃Cl₂NO₅ 
• 1290540-93-0 C₁₈H₂₅Cl₂NO₇S 
• 1290540-95-2 C₁₇H₂₁NO₄ 
• 1290540-83-8 C₂₅H₂₃F₆NO₄ 
• 1290540-84-9 C₂₄H₂₄F₃NO₄ 
• 1290540-85-0 C₂₃H₂₀F₅NO₄ 
• 1290540-86-1 C₂₉H₃₅F₂NO₄ 
• 1339077-36-9 C₃₁H₄₁NO₄ 

Relevant articles and documents

Tandem oxidative radical fragmentation-rearrangement of 2-amino-1,3-benzylidene acetals: A short entry to densely functionalised fully differentiated oxazolidinones

The discovery of a novel tandem fragmentation-rearrangement process from N-Boc-protected benzylidene acetals is reported. The reaction proceeds via free-radical initiation and terminates through a 5-exo-tet ionic fragmentation process leading to biologically useful, densely functionalised oxazolidinones.

A convergent synthesis of the immunosuppressant FTY720 employing aqueous Wittig chemistry

A short, convergent synthesis of the immunosuppressant FTY720 is described involving the use of 4-hydroxymethylbenzaldehyde as a pivotal intermediate. A double Wittig strategy was developed to connect this dual-functional aldehyde with an alkyl-tether and to a readily available TRIS-derivative leading to an efficient synthesis of the target molecule.

The total synthesis of antrimycin D(v)

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