387871-69-4

Basic information

• Product Name: allyl 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propanoate
• CAS NO: 387871-69-4
• Molecular Weight: 782.934
• Mol File: 387871-69-4.mol

Chemical Properties

• CAS DataBase Reference: allyl 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propanoate(387871-69-4)
• EPA Substance Registry System: allyl 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propanoate(387871-69-4)

Safety Data

• Hazardous Substances Data: 387871-69-4(Hazardous Substances Data)

Upstream product

• 387871-67-2 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propan-1-ol 
• 387871-64-9 2-benzoyloxymethyl-N-(tert-butyloxycarbonyl)-2-(4-methoxytrityloxy)methyl-N'-phthaloylpropane-1,3-diamine 
• 387871-63-8 2-benzoyloxymethyl-2-(tert-butyloxycarbonylamino)methyl-3-(4-methoxytrityloxy)propan-1-ol 
• 387871-62-7 5-(tert-butyloxycarbonylamino)methyl-5-(4-methoxytrityloxy)methyl-2-phenyl-1,3-dioxane 
• 387871-66-1 2-aminomethyl-2-[N-(tert-butyloxycarbonyl)amino]methyl-3-(4-methoxytrityloxy)propanol 
• 387871-61-6 5-aminomethyl-5-(4-methoxytrityloxy)methyl-2-phenyl-1,3-dioxane 
• 387871-59-2 5-hydroxymethyl-5-(4-methoxytrityloxy)methyl-2-phenyl-1,3-dioxane 
• 14470-28-1 mono-4-methoxytrityl chloride 
• 2425-41-4 5,5-dihydroxymethyl-2-phenyl-1,3-dioxane 
• 106-95-6 allyl bromide 
• 387871-68-3 2-(tert-butyloxycarbonylamino)methyl-2-(9-fluorenylmethoxycarbonylamino)methyl-3-(4-methoxytrityloxy)propanoic acid 
• 387871-65-0 2-(tert-butyloxycarbonylamino)methyl-3-(4-methoxytrityloxy)-2-phthalimidomethylpropan-1-ol 
• 387871-60-5 5-(4-methoxytrityloxy)methyl-2-phenyl-5-phthalimidomethyl-1,3-dioxane 

Relevant articles and documents

Synthesis of orthogonally protected bis(aminomethyl)malonic acid, and its use as a key building block in the preparation of cyclic peptide conjugates of 2-N-alkyl-1,2,3,4-tetrahydroisoquinoline on a solid support

Orthogonally protected bis(aminomethyl)malonic acid (1) was synthesized and used as a key building block for the construction of cyclic peptide conjugates on a solid support. The applicability of the building block was demonstrated by preparation of 19 ba