Taiy Chemical
N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine
Product Name fmoc-O-tert-butyl-L-tyrosine
Synonyms:8879 N-(9-Fluorenyl Methoxy Carbonyl)-O-Tertbutyl-L-Tyrosine; N-fmoc-O-T-butyl-L-tyrosine; Fmoc-Tyr(tBu)-OH; Fmoc-Tyr(But)-OH; N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine; O-tert-butyl-N-[(9H-fluoren-9-ylmethoxy)carbonyl]tyrosine; Fmoc-O-tert.butyl-L-tyrosine; Fmoc-Tyr(OtBu)-OH; Fmoc-L-Tyr(tBu)-OH; Tyr(tBu)
CAS RN. 71989-38-3
EINECS 276-262-7
Molecular Weight 459.5336
Molecular Formula C28H29NO5
Density 1.218g/cm3
Melting Point(℃) 153-156℃
Boiling Point(℃) 658.2°C at 760 mmHg
Flash Point(℃) 351.9°C
refractive_index 1.599
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FAQ
What is N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine?
N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine, also known as Fmoc-O-t-butyl-L-tyrosine, is a derivative of the amino acid tyrosine. It is commonly used in peptide synthesis as a building block for creating peptides with specific sequences.

What are the key features of N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine?
One of the key features of N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine is its Fmoc protecting group, which allows for selective deprotection during peptide synthesis. The O-t-butyl group also provides added protection to the tyrosine side chain.

How is N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine commonly used in peptide synthesis?
N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine is typically used as a building block in solid-phase peptide synthesis. It is often incorporated into the peptide chain at specific positions to introduce tyrosine residues with protected side chains.

What are the advantages of using N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine in peptide synthesis?
One advantage of using N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine is its selective deprotection property, which allows for efficient synthesis of complex peptides with minimal side reactions. The O-t-butyl group also offers additional protection to the tyrosine side chain, reducing the risk of undesired modifications.

Are there any specific precautions or considerations when working with N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine in peptide synthesis?
It is important to handle N-alpha-(9-fluorenylmethyloxycarbonyl)-O-t-butyl-L-tyrosine with care to avoid exposure to skin or eyes. Proper safety equipment, such as gloves and goggles, should be worn when handling this compound. Additionally, due to its sensitive nature, storage conditions should be closely monitored to prevent degradation or contamination.
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