Fmoc-O-tert-butyl-L-serine

• CAS: 71989-33-8
• Catalog Number: ACM71989338
• Category: Other Products
• Molecular Weight: 383.44
• Molecular Formula: C₂₂H₂₅NO₅
• Synonyms: N-FMOC-O-TERT-BUTYL-L-SERINE;N-FMOC-SER(T-BU)-OH;N-FMOC-O-T-BUTYL-L-SERINE;N-FMOC-T-BUTYL-L-SER;N-ALPHA-FMOC-O-TERT-BUTYL-L-SERINE;N-ALPHA-FMOC-O-T-BUTYL-L-SERINE;N-9-FLUORENYLMETHYLOXYCARBONYL-O-TERT-BUTYL-L-SERINE;N-9-FLUORENYLMETHYLOXYCARBONYL-O-T-BUTYL-L-SERINE
• Melting Point: 130.5-135.5°C(lit.)
• Hazard Statements: Xi
• Safety Description: 24/25-36/37/39-27-26

Custom Q&A

What is the molecular formula of Fmoc-O-tert-butyl-L-serine?

The molecular formula of Fmoc-O-tert-butyl-L-serine is C22H25NO5.

When was Fmoc-O-tert-butyl-L-serine first created and modified?

Fmoc-O-tert-butyl-L-serine was first created on July 19, 2005, and last modified on December 30, 2023.

What is the IUPAC name of Fmoc-O-tert-butyl-L-serine?

The IUPAC name of Fmoc-O-tert-butyl-L-serine is (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[(2-methylpropan-2-yl)oxy]propanoic acid.

What is the InChIKey of Fmoc-O-tert-butyl-L-serine?

The InChIKey of Fmoc-O-tert-butyl-L-serine is REITVGIIZHFVGU-IBGZPJMESA-N.

What is the Canonical SMILES of Fmoc-O-tert-butyl-L-serine?

The Canonical SMILES of Fmoc-O-tert-butyl-L-serine is CC(C)(C)OCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13.

What is the molecular weight of Fmoc-O-tert-butyl-L-serine?

The molecular weight of Fmoc-O-tert-butyl-L-serine is 383.4 g/mol.

How many hydrogen bond donor counts does Fmoc-O-tert-butyl-L-serine have?

Fmoc-O-tert-butyl-L-serine has 2 hydrogen bond donor counts.

What is the exact mass of Fmoc-O-tert-butyl-L-serine?

The exact mass of Fmoc-O-tert-butyl-L-serine is 383.17327290 g/mol.

How many rotatable bond counts does Fmoc-O-tert-butyl-L-serine have?

Fmoc-O-tert-butyl-L-serine has 8 rotatable bond counts.

What is the topological polar surface area of Fmoc-O-tert-butyl-L-serine?

The topological polar surface area of Fmoc-O-tert-butyl-L-serine is 84.9 Ų.

Synthetic Use

Upstream Synthesis Route 1

• 146346-72-7

• 71989-33-8

Reference: [1] Tetrahedron Letters, 1992, vol. 33, # 49, p. 7605 - 7608
[2] Organic Letters, 2005, vol. 7, # 9, p. 1723 - 1724

Upstream Synthesis Route 2

• 129460-16-8

• 71989-33-8
• 73724-45-5

Reference: [1] Tetrahedron Letters, 2001, vol. 42, # 31, p. 5163 - 5165

Upstream Synthesis Route 3

• 18822-58-7
• 102774-86-7

• 71989-33-8

Reference: [1] Liebigs Annalen der Chemie, 1988, p. 1095 - 1098

Downstream Synthesis Route 1

• 35661-39-3
• 122889-11-6
• 71989-33-8

• 849063-77-0

Reference: [1]Journal of Organic Chemistry,2005,vol. 70,p. 1691 - 1697

* For details of the synthesis route, please refer to the original source to ensure accuracy.