681287-04-7

Basic information

• Product Name: cyclo-[SAA(Piv)-Val-Orn(Boc)-Leu-^DPhe-Pro-Val-Orn(Boc)-Leu]
• Synonyms: cyclo-[SAA(Piv)-Val-Orn(Boc)-Leu-^DPhe-Pro-Val-Orn(Boc)-Leu]
• CAS NO: 681287-04-7
• Molecular Weight: 1340.67
• Mol File: 681287-04-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: cyclo-[SAA(Piv)-Val-Orn(Boc)-Leu-^DPhe-Pro-Val-Orn(Boc)-Leu](CAS DataBase Reference)
• NIST Chemistry Reference: cyclo-[SAA(Piv)-Val-Orn(Boc)-Leu-^DPhe-Pro-Val-Orn(Boc)-Leu](681287-04-7)
• EPA Substance Registry System: cyclo-[SAA(Piv)-Val-Orn(Boc)-Leu-^DPhe-Pro-Val-Orn(Boc)-Leu](681287-04-7)

Safety Data

• Hazardous Substances Data: 681287-04-7(Hazardous Substances Data)

Upstream product

• 68858-20-8 Fmoc-Val-OH 
• 35661-60-0 Fmoc-Leu-OH 
• 109425-55-0 Fmoc-Orn(Boc)-OH 
• 681287-02-5 2,5-anhydro-6-azido-6-deoxy-4-O-pivaloyl-D-gluconic acid 
• 813436-33-8 2,5-anhydro-6-azido-6-deoxy-1,3-O-isopropylidene-D-glucitol 
• 3282-30-2 pivaloyl chloride 

Downstream Products

• 681287-05-8 C₆₂H₁₀₁N₁₁O₁₆ 

Relevant articles and documents

An Unusual Reverse Turn Structure Adopted by a Furanoid Sugar Amino Acid Incorporated in Gramicidin S

A new reverse turn, replacing one of the native type II′ β-turns in the cyclic peptide antibiotic gramicidin S, induced by a furanoid sugar amino acid is revealed. The C3-hydroxyl function plays a pivotal role by acting as a H-bond acceptor, co