903523-86-4

Basic information

• Product Name: (9S,12S,15S)-4-benzyloxy-15-dibenzylamino-12-(4-hydroxybenzyl)-11,14-dioxo-2-oxa-10,13-diazatricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid benzyl ester
• Synonyms: (9S,12S,15S)-4-benzyloxy-15-dibenzylamino-12-(4-hydroxybenzyl)-11,14-dioxo-2-oxa-10,13-diazatricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid benzyl ester
• CAS NO: 903523-86-4
• Molecular Weight: 866.026
• Mol File: 903523-86-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (9S,12S,15S)-4-benzyloxy-15-dibenzylamino-12-(4-hydroxybenzyl)-11,14-dioxo-2-oxa-10,13-diazatricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (9S,12S,15S)-4-benzyloxy-15-dibenzylamino-12-(4-hydroxybenzyl)-11,14-dioxo-2-oxa-10,13-diazatricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid benzyl ester(903523-86-4)
• EPA Substance Registry System: (9S,12S,15S)-4-benzyloxy-15-dibenzylamino-12-(4-hydroxybenzyl)-11,14-dioxo-2-oxa-10,13-diazatricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid benzyl ester(903523-86-4)

Safety Data

• Hazardous Substances Data: 903523-86-4(Hazardous Substances Data)

Upstream product

• 903523-85-3 (S)-3-[4-benzyloxy-3-(4-{(S)-2-[(S)-1-tert-butoxycarbonyl-2-(4-hydroxy-phenyl)ethylcarbamoyl]-2-dibenzylaminoethyl}phenoxy)phenyl]-2-(tritylamino)-propionic acid benzyl ester 
• 224824-21-9 N-(tert-butyloxycarbonyl)-3-(3-hydroxy-4-benzyloxyphenyl)-L-alanine benzyl ester 
• 903523-87-5 (S)-3-(4-{2-Benzyloxy-5-[(S)-2-benzyloxycarbonyl-2-(trityl-amino)-ethyl]-phenoxy}-phenyl)-2-dibenzylamino-propionic acid 
• 903523-84-2 (S)-3-{4-benzyloxy-3-[4-((S)-2-dibenzylamino-2-methoxycarbonylethyl)phenoxy]phenyl}-2-(tritylamino)propionic acid benzyl ester 
• 903523-81-9 (S)-3-(4-benzyloxy-3-hydroxyphenyl)-2-(tritylamino)propionic acid benzyl ester 

Downstream Products

• 108890-90-0 K-13 

Relevant articles and documents

Mild and nonracemizing conditions for Ullmann-type diaryl ether formation between aryl iodides and tyrosine derivatives

CuI/N,N-dimethylglycine-catalyzed coupling reaction of L-tyrosine derivatives and L-phenylalanine-derived iodides in the presence of Cs 2CO3 works at 90 °C to provide the corresponding diaryl ether. Partial racemization occurs when N