1026486-04-3

Basic information

• Product Name: (S)-2-(Benzhydrylidene-amino)-3-(2-benzyloxy-5-nitro-phenyl)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one
• Synonyms: (S)-2-(Benzhydrylidene-amino)-3-(2-benzyloxy-5-nitro-phenyl)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one
• CAS NO: 1026486-04-3
• Molecular Weight: 677.821
• Mol File: 1026486-04-3.mol

Chemical Properties

• CAS DataBase Reference: (S)-2-(Benzhydrylidene-amino)-3-(2-benzyloxy-5-nitro-phenyl)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(Benzhydrylidene-amino)-3-(2-benzyloxy-5-nitro-phenyl)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(1026486-04-3)
• EPA Substance Registry System: (S)-2-(Benzhydrylidene-amino)-3-(2-benzyloxy-5-nitro-phenyl)-1-((1R,5S,7S)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(1026486-04-3)

Safety Data

• Hazardous Substances Data: 1026486-04-3(Hazardous Substances Data)

Upstream product

• 168702-54-3 (2-(benzyloxy)-5-nitrophenyl)methanol 
• 100-39-0 benzyl bromide 
• 39224-61-8 2-hydroxy-5-nitrobenzyl alcohol 
• 168702-56-5 2-(Benzyloxy)-5-nitrobenzyl iodide 

Downstream Products

• 1026414-80-1 (S)-2-[(S)-3-(2-Benzyloxy-5-nitro-phenyl)-2-tert-butoxycarbonylamino-propionylamino]-propionic acid methyl ester 
• 168702-68-9 Ac-L-o-Nip(Bn)-Ala-OMe 
• 1027951-56-9 (S)-2-[(S)-2-Amino-3-(2-benzyloxy-5-nitro-phenyl)-propionylamino]-propionic acid methyl ester 
• 168702-64-5 Boc-L-o-Nip(Bn) 
• 1810074-88-4 L-o-Tyr hydrochloride 
• 1027892-43-8 (S)-2-[(S)-2-Acetylamino-3-(5-amino-2-hydroxy-phenyl)-propionylamino]-propionic acid methyl ester 
• 1027149-76-3 (S)-2-Amino-3-(2-benzyloxy-5-nitro-phenyl)-propionic acid 

Relevant articles and documents

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4-Diazocyclohexa-2,5-dienone-based amino acids m-Dip and o-Dip were designed for building up photoactivatable peptides.Their stable precursors L-3-alanine (L-m-Nip(Bn)) and L-3-alanine (L-o-Nip(Bn)