55070-01-4

Basic information

• Product Name: AM toxin I
• Synonyms: AM toxin I
• CAS NO: 55070-01-4
• Molecular Formula: C23H31N3O6
• Molecular Weight: 445.50874
• Mol File: 55070-01-4.mol

Chemical Properties

• Boiling Point: 807.7°C at 760 mmHg
• Flash Point: 442.3°C
• Appearance: /
• Density: 1.2g/cm³
• Vapor Pressure: 3.94E-26mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: AM toxin I(CAS DataBase Reference)
• NIST Chemistry Reference: AM toxin I(55070-01-4)
• EPA Substance Registry System: AM toxin I(55070-01-4)

Safety Data

• Hazardous Substances Data: 55070-01-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C23H31N3O6/c1-13(2)19-22(29)26-18(8-6-7-16-9-11-17(31-5)12-10-16)21(28)24-14(3)20(27)25-15(4)23(30)32-19/h9-13,15,18-19H,3,6-8H2,1-2,4-5H3,(H,24,28)(H,25,27)(H,26,29)/t15-,18-,19-/m0/s1

Upstream product

• 56047-44-0 (S)-2-amino-5-(4-methoxyphenyl)pentanoic acid 
• 60008-23-3 Boc-L-Ala-L-Hmb-OBzl 
• 65138-05-8 (S)-2-hydroxy-3-methylbutyric acid benzyl ester 
• 62732-54-1 2-Acetylamino-5-(4-methoxy-phenyl)-pentanoic acid 
• 62732-50-7 2-Acetylamino-2-[3-(4-methoxy-phenyl)-propyl]-malonic acid diethyl ester 
• 62732-53-0 2-Acetylamino-2-[3-(4-methoxy-phenyl)-propyl]-malonic acid 
• 57293-19-3 3-(4-methoxyphenyl)propyl bromide 
• 5406-18-8 3-(p-methoxyphenyl)-1-propanol 
• 1929-29-9 3-(4-methoxyphenyl)propanoic acid 
• 17407-55-5 (S)-2-Hydroxy-3-methylbutanoic acid 
• 178861-43-3 (3S,6S,9S,12S)-12-Isopropyl-9-[3-(4-methoxy-phenyl)-propyl]-3-methyl-6-phenylselanylmethyl-1-oxa-4,7,10-triaza-cyclododecane-2,5,8,11-tetraone 
• 178861-45-5 Boc-L-Amp-O-tBu 
• 178861-44-4 Boc-L-Amp-OH 
• 60008-24-4 Boc-L-Ala-L-Hmb-OH 

Relevant articles and documents

Facile Syntheses of AM-toxins and Analogs as Cyclic Depsipeptides by the Solid-phase Method

The cyclic depsipeptides, AM-toxins I and II and AM-toxin I analogs, were efficiently and rapidly prepared by the Fmoc-based solid-phase method for the synthesis of linear depsipeptides, with N-pyridin-1-ylmethylene>-N-methylmethanaminium hexafluorophosphate N-oxide (HATU) being used for their subsequent cyclization. - Keywords: Am-toxin; host-specific toxin; cyclic depsipeptide; solid-phase synthesis; HATU.

β-Phenylselenoalanine as a dehydroalanine precursor-efficient synthesis of alternariolide (AM-toxin I)

Alternariolide (AM-toxin) is synthesized in 44% overall yield from L-2-amino-5-(4-methoxyphenyl)pentanoic acid; D-β-phenylselenoalanine is used as the dehydroalanine precursor.