84506-41-2

Basic information

• Product Name: methyl (2R)-3-azido-2-methylpropanoate
• Synonyms: Methyl (2R)-3-azido-2-methylpropanoate; propanoic acid, 3-azido-2-methyl-, methyl ester, (2R)-
• CAS NO: 84506-41-2
• Molecular Formula: C₅H₉N₃O₂
• Molecular Weight: 143.1439
• Mol File: 84506-41-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: methyl (2R)-3-azido-2-methylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (2R)-3-azido-2-methylpropanoate(84506-41-2)
• EPA Substance Registry System: methyl (2R)-3-azido-2-methylpropanoate(84506-41-2)

Safety Data

• Hazardous Substances Data: 84506-41-2(Hazardous Substances Data)

Upstream product

• 84341-94-6 methyl (R)-2-methyl-3-[(4'-toluenesulfonyl)oxy]propionate 
• 72657-23-9 methyl (R)-3-hydroxy-2-methylpropionate 
• 866760-16-9 (R)-methyl-3-methanesulfonyloxy-2-methyl-propionate 

Downstream Products

• 182486-32-4 (R)-methyl 3-{[(tert-butoxy)carbonyl]amino}-2-methylpropionate 

Relevant articles and documents

Oligomers of N-Substituted β2-Homoalanines: Peptoids with Backbone Chirality

A new class of peptoid-based peptidomimetics composed of oligomers of N-substituted β2-homoalanines is reported. Design, solid-phase synthesis, and preliminary circular dichroism studies of oligomers of N-alkylated β2-homoalanines co

A series of 23,24-dihydrodiscodermolide analogues with simplified lactone regions

A collection of seven new 23,24-dihydrodiscodermolide analogues have been synthesized with modifications to the lactone ring, some of which show antiproliferative activities similar to discodermolide.

Asymmetric syntheses of potent antitumor macrolides cryptophycin B and arenastatin A

Efficient and highly stereoselective syntheses of cryptophycin B and arenastatin A, potent cytotoxic agents, are described. An ester-derived titanium enolate mediated syn-aldol reaction was employed to generate the stereocenters C-5 and C-6. The route is convergent and provides a convenient access to the synthesis of structural variants of cryptophycins as well as members of its family. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004).