Fmoc-D-Pro-OH

Base Information

• Chemical Name: Fmoc-D-Pro-OH
• CAS No.: 101555-62-8
• Molecular Formula: C₂₀H₁₉NO₄
• Molecular Weight: 337.375
• Hs Code.: 2933 99 80
• European Community (EC) Number: 691-539-6
• DSSTox Substance ID: DTXSID20906313
• Nikkaji Number: J2.650.798G
• Wikidata: Q72478829
• Mol file: 101555-62-8.mol

Synonyms:Fmoc-D-Pro-OH;101555-62-8;Fmoc-D-proline;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-proline;(2R)-1-(9H-fluoren-9-ylmethoxycarbonyl)pyrrolidine-2-carboxylic acid;MFCD00077067;(2R)-1-{[(9H-fluoren-9-yl)methoxy]carbonyl}pyrrolidine-2-carboxylic acid;N-Fmoc-D-proline;N-Fmoc-Pro-OH ( N-Fmoc-L-proline);FMOC-D-PRO;Fmoc-D-Pro-OH.nH2O;SCHEMBL119560;DTXSID20906313;Fmoc-D-Pro-OH, >=98.0%;AKOS015924247;AM82195;CS-W009840;HY-W009124;AC-24079;AC-24080;AS-12717;N-(9-Fluorenylmethoxycarbonyl)-D-proline;F0606;EN300-81320;F10527;M03373;1-{[(9H-Fluoren-9-yl)methoxy]carbonyl}proline;(((9H-Fluoren-9-yl)methoxy)carbonyl)-D-proline;A800405;J-300223;Q-101838;(R)-1-(((9H-FLUOREN-9-YL)METHOXY)CARBONYL)PYRROLIDINE-2-CARBOXYLIC ACID

Chemical Property of Fmoc-D-Pro-OH

Chemical Property:

• Appearance/Colour: White solid
• Melting Point: 110-116 °C
• Refractive Index: 32 ° (C=1, DMF)
• Boiling Point: 548.6 °C at 760 mmHg
• PKA: 3.95±0.20(Predicted)
• Flash Point: 285.6 °C
• PSA: 66.84000
• Density: 1.328 g/cm³
• LogP: 3.42240
• Storage Temp.: 2-8°C
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 337.13140809
• Heavy Atom Count: 25
• Complexity: 500

Purity/Quality:

99% ^*data from raw suppliers

Fmoc-D-proline 99+% ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O
• Isomeric SMILES: C1C[C@@H](N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O
• Uses: In organic synthesis, N-Fmoc-D-proline are often employed as important intermediates in various areas such as peptide synthesis, asymmetric synthesis, medicinal chemistry, and polymer chemistry.