704910-26-9

Basic information

• Product Name: L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-seryl-, 1,1-dimethylethyl ester
• CAS NO: 704910-26-9
• Molecular Formula: C31H34N2O6
• Molecular Weight: 530.621
• Mol File: 704910-26-9.mol

Chemical Properties

• CAS DataBase Reference: L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-seryl-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-seryl-, 1,1-dimethylethyl ester(704910-26-9)
• EPA Substance Registry System: L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-seryl-, 1,1-dimethylethyl ester(704910-26-9)

Safety Data

• Hazardous Substances Data: 704910-26-9(Hazardous Substances Data)

Upstream product

• 704910-17-8 N-Fmoc-O-allylserine 
• 15100-75-1 L-phenylalanine tert-butyl ester hydrochloride 
• 704910-22-5 2-[3-allyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-3-phenyl-propionic acid tert-butyl ester 

Downstream Products

• 704910-22-5 2-[3-allyloxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionylamino]-3-phenyl-propionic acid tert-butyl ester 

Relevant articles and documents

CpRuIIPF6/quinaldic acid-catalyzed chemoselective allyl ether cleavage. A simple and practical method for hydroxyl deprotection

Matrix presented. A cationic CpRuII complex in combination with quinaldic acid shows high reactivity and chemoselectivity for the catalytic deprotection of hydroxyl groups protected as allyl ethers. The catalyst operates in alcoholic solvents without the need for any additional nucleophiles, satisfying the practical requirements of operational simplicity, safety, and environmental friendliness. The wide applicability of this deprotection strategy to a variety of multifunctional molecules, including peptides and nucleosides, may provide new opportunities in protective group chemistry.