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Fmoc-D-proline

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Fmoc-D-proline manufacturers

  • Fmoc-D-proline
  • Fmoc-D-proline pictures
  • 2026-09-17
  • CAS:101555-62-8
  • Min. Order: 1kg
  • Purity: 99%min HPLC
  • Supply Ability: 100kg
  • Fmoc-D-proline
  • Fmoc-D-proline pictures
  • $1.00
  • 2019-07-06
  • CAS:101555-62-8
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 20kg
Fmoc-D-proline Basic information
Product Name:Fmoc-D-proline
Synonyms:N-ALPHA-FMOC-D-PROLINE;N-(9-FLUORENYLMETHOXYCARBONYL)-D-PROLINE;N-(9-FLUORENYLMETHOXYCARBONYL)-D-PYRROLIDINE-2-CARBOXYLIC ACID;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-PROLINE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-PROLINE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-PROLINE MONOHYDRATE;9-FLUORENYLMETHOXYCARBONYL-D-PROLINE;FMOC-D-PROLINE
CAS:101555-62-8
MF:C20H19NO4
MW:337.37
EINECS:1806241-263-5
Product Categories:Amino Acids (N-Protected);Biochemistry;Fmoc-Amino Acids;Fmoc-Amino acid series;Proline [Pro, P];Fmoc-Amino Acids and Derivatives;Amino Acids
Mol File:101555-62-8.mol
Fmoc-D-proline Structure
Fmoc-D-proline Chemical Properties
Melting point 110-116°C
Boiling point 548.6±43.0 °C(Predicted)
density 1.328±0.06 g/cm3(Predicted)
refractive index 32 ° (C=1, DMF)
storage temp. 2-8°C
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form powder to crystal
pka3.95±0.20(Predicted)
color White to Light yellow
Optical Rotation[α]/D +31.0±3.0°, c = 1 in DMF
BRN 5856698
Major Applicationpeptide synthesis
InChIInChI=1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m1/s1
InChIKeyZPGDWQNBZYOZTI-GOSISDBHSA-N
SMILESN1(C(OCC2C3=C(C=CC=C3)C3=C2C=CC=C3)=O)CCC[C@@H]1C(O)=O
CAS DataBase Reference101555-62-8(CAS DataBase Reference)
Safety Information
Safety Statements 22-24/25
WGK Germany 3
HS Code 2933 99 80
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Fmoc-D-proline Usage And Synthesis
Chemical PropertiesWhite powder
UsesIn 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.
reaction suitabilityreaction type: Fmoc solid-phase peptide synthesis
SynthesisD-proline was added to a round-bottomed flask, 10% aqueous sodium carbonate was added and stirred to dissolve, then dioxane was added, and a 10% dioxane solution of 9-fluorenylmethoxycarbonyl chloride was slowly added dropwise into the reaction solution under an ice bath, and after the dropwise addition was completed the reaction was carried out in an ice bath for 2 hours, and then at room temperature for 8 hours, and the reaction was diluted with the addition of water, and the extract was carried out with ether 4 times, the aqueous layer was placed in an ice bath, the pH was adjusted with concentrated hydrochloric acid until the Congo red paper showed blue, placed in a refrigerator overnight, the white precipitate was extracted with ethyl acetate, the combined organic solution was washed with water, the organic layer was dried with anhydrous magnesium sulphate, and the product FMOC-D-proline was obtained by pumping dry.
Fmoc-D-proline Preparation Products And Raw materials
Tag:Fmoc-D-proline(101555-62-8) Related Product Information
Fmoc-D-phenylalanine Fmoc-Met-OH Fmoc-Lys(Boc)-OH 9-Fluorenylmethyl chloroformate L-Proline Fmoc-Phe-OH cis-4-Hydroxy-L-proline Fmoc-Asp(OtBu)-OH D-Proline Nalpha-Fmoc-Ndelta-trityl-L-glutamine L-Fmoc-Aspartic acid alpha-tert-butyl ester 9-Fluorenemethanol Fmoc-OSu L-Proline-(4-3H(n)) Methoxycarbonylsulfenyl chloride Fmoc-Thr(tBu)-ol Fmoc-D-Asn(Trt)-OH Fmoc-5-aminopentanoic acid