143327-81-5

Basic information

• Product Name: Carbamic acid, [1-[[4-(phenylmethoxy)phenyl]methyl]-2-propynyl]-, 1,1-dimethylethyl ester, (S)-
• CAS NO: 143327-81-5
• Molecular Formula: C22H25NO3
• Molecular Weight: 351.445
• Mol File: 143327-81-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [1-[[4-(phenylmethoxy)phenyl]methyl]-2-propynyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [1-[[4-(phenylmethoxy)phenyl]methyl]-2-propynyl]-, 1,1-dimethylethyl ester, (S)-(143327-81-5)
• EPA Substance Registry System: Carbamic acid, [1-[[4-(phenylmethoxy)phenyl]methyl]-2-propynyl]-, 1,1-dimethylethyl ester, (S)-(143327-81-5)

Safety Data

• Hazardous Substances Data: 143327-81-5(Hazardous Substances Data)

Upstream product

• 4202-14-6 dimethyl (2-oxopropyl)phosphonate 
• 82689-15-4 O-benzyl-N-(tert-butoxycarbonyl)-L-tyrosinal 

Downstream Products

• 1265145-93-4 C₃₃H₄₆N₂O₆ 
• 1265146-05-1 C₂₇H₃₁NO₃S 
• 1265146-04-0 C₃₂H₄₂N₂O₅S 
• 1265145-94-5 C₃₂H₄₄N₂O₆S 
• 1265146-11-9 C₂₄H₂₆N₂O₂ 
• 1265146-03-9 C₂₈H₃₃NO₃ 
• 1265146-02-8 C₃₃H₄₄N₂O₅ 

Relevant articles and documents

Pyrrole-based scaffolds for turn mimics

Two amino acid derived synthons were combined to give homopropargylic amines 2. Platinum dichloride was used to cyclize these intermediates into pyrroles 3 which collapsed to the target secondary structure mimics 1 on treatment with base. Side chains of these compounds overlay with an idealized type 1 β-turn and with an inverse γ-turn.(Figure Presented)