34048-58-3

Basic information

• Product Name: N-((1S)-neomenthyl)-formamide
• CAS NO: 34048-58-3
• Molecular Weight: 183.294
• Mol File: 34048-58-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-((1S)-neomenthyl)-formamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-((1S)-neomenthyl)-formamide(34048-58-3)
• EPA Substance Registry System: N-((1S)-neomenthyl)-formamide(34048-58-3)

Safety Data

• Hazardous Substances Data: 34048-58-3(Hazardous Substances Data)

Upstream product

• 540-69-2 ammonium formate 
• 1196-31-2 (1R,4R)-(+)-isomenthone 
• 259826-43-2 (1S,3R,4R)-3-azidomenthane 
• 2258-42-6 formyl acetic anhydride 
• 2216-54-8 L-menthylamine 
• 109-94-4 formic acid ethyl ester 
• 64-18-6 formic acid 
• 107535-12-6 (1S,2S,4R)-2-azido-1-isopropyl-4-methylcyclohexane 
• 7231-40-5 (+)-(1R,3S,4S)-neomenthylamine 

Downstream Products

• 7231-40-5 (+)-(1R,3S,4S)-neomenthylamine 
• 1446348-66-8 C₁₁H₁₉N 
• 1446348-69-1 C₁₁H₁₉N 
• 1446348-70-4 C₁₆H₃₀N₂O₃ 
• 39633-53-9 (1R)-neomenthyl isocyanate 
• 56087-04-8 salicylidene-D-neomenthylamine 
• 5033-86-3 3c-Nitro-1r-methyl-4t-isopropyl-cyclohexan (Nitromenthan) 

Relevant articles and documents

A biomimetic approach to terpenes isolated from marine sponges: A Ugi coupling reaction in a hypothetical biosynthesis

A unique pathway for the biosynthesis of marine sponge terpenes is proposed. Based on this proposal, a biomimetic approach using a Ugi coupling reaction has been designed and applied to the efficient construction of the right-side, peptide-like portions of boneratamides and exigurin. Georg Thieme Verlag Stuttgart - New York.