1613450-06-8

Basic information

• Product Name: tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate
• Synonyms: tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate
• CAS NO: 1613450-06-8
• Molecular Weight: 359.441
• Mol File: 1613450-06-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate(1613450-06-8)
• EPA Substance Registry System: tert-butyl 2-(benzylamino)-2-(4-fluorobenzyl)-3-hydroxypropanoate(1613450-06-8)

Safety Data

• Hazardous Substances Data: 1613450-06-8(Hazardous Substances Data)

Upstream product

• 99184-99-3 2-phenyloxazoline-4-carboxylic acid 
• 116956-53-7 sodium 2-phenyloxazoline-4-carboxylate 
• 100-47-0 benzonitrile 
• 55044-06-9 methyl 2-phenyl-2-oxazoline-4-carboxylate 
• 5333-86-8 ethyl benzimidate hydrochloride 

Downstream Products

• 1613450-09-1 tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2-oxo-1,2,3-oxathiazolidine-4-carboxylate 
• 1613450-12-6 tert-butyl 3-benzyl-4-(4-fluorobenzyl)-2,2-dioxo-1,2,3-oxathiazolidine-4-carboxylate 
• 1613450-15-9 tert-butyl 2-benzylamino-3-((R)-2-(tert-butoxycarbonylamino)-3-methoxy-3-oxopropylthio)-2-(4-fluorobenzyl)propanoate 

Relevant articles and documents

Synthesis of protected α-alkyl lanthionine derivatives

Protected α-alkyl lanthionine derivatives were synthesized in five steps starting from a known phenyloxazoline precursor. This approach involved the synthesis of a family of substituted cyclic sulfamidates and their regioselective opening by nucleophilic attack with a protected cysteine. This efficient multistep strategy affords various α-alkylated lanthionine derivatives in high yields.