Lot numbers can be found on the outside label of a product:
Fmoc-Ile-OH
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CAS No. 71989-23-6
- Cat. No. CS-W020667
- Purity≥98%
- MDL No.MFCD00037125
*For research and further manufacturing use only, not for direct human use.
Structure of 71989-23-6
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General Information
- CAS No. 71989-23-6
- Cat. No. CS-W020667
- Purity ≥98%
- MDL No. MFCD00037125
- Storage Store at room temperature
- Shipping Room temperature in continental US; may vary elsewhere.
- Molecular Formula C₂₁H₂₃NO₄
- Molecular Weight None
- Synonym(s) Fmoc-L-isoleucine
- SMILES CC[C@H](C)[C@@H](C(O)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O
Description
Fmoc-Ile-OH is a bench-stable, moisture-tolerant amino acid derivative featuring a fluorenylmethoxy carbonyl (Fmoc) protecting group and a side chain bearing a branched isopropyl moiety. This structure enables efficient coupling in solid-phase peptide synthesis, where the Fmoc group facilitates selective deprotection under mild basic conditions. The protected side chain remains inert during standard coupling protocols, ensuring high fidelity in sequence assembly.
Synthesis
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Route1
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73-32-5 -
In-stock
82911-69-1 - ~89%
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In-stock
71989-23-6
References
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Raydnov, M. G.; Klimenko, L. V.; Mitin, Yu. V. Russian Journal of Bioorganic Chemistry, 1999 , vol. 25, # 5 p. 283 - 287 Bioorganicheskaya Khimiya, 1999 , vol. 25, # 5 p. 323 - 328
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Route2
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73-32-5
- ~69%
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In-stock
71989-23-6
References
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Chinchilla, Rafael; Dodsworth, David; Najera, Carmen; Soriano, Jose Tetrahedron Letters, 2001 , vol. 42, # 43 p. 7579 - 7581
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Route3
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73-32-5
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In-stock
88744-04-1 - ~82%
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In-stock
71989-23-6
References
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Schoen, Istvan; Kisfaludy, Lajos Synthesis, 1986 , # 4 p. 303 - 305
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Safety Information
Download SDS|
GHS Pictogram :
N/A
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GHS No : N/A
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Signal Word : N/A
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : N/A
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Precautionary Statements : N/A
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Quality Control
Computational Chemistry Data
- TPSA 75.63
- LogP 4.0244
- H_Acceptors 3
- H_Donors 2
- Rotatable_Bonds 6
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Key Words
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