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Fmoc-Gly-OH

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Related articles

Fmoc-Gly-OH Basic information
Product Name:Fmoc-Gly-OH
Synonyms:9-FLUORENYLMETHOXYCARBONYL-GLYCINE;FMOC-L-GLY-OH;FMOC-L-GLY;FMOC-L-GLYCINE;FMOC-GLYCINE;FMOC-GLY;FMOC-GLY-OH;F-FMOC-GLYCINE
CAS:29022-11-5
MF:C17H15NO4
MW:297.31
EINECS:249-373-3
Product Categories:Glycine [Gly, G];Fmoc-Amino Acids and Derivatives;Amino Acids (N-Protected);Biochemistry;Fmoc-Amino Acids;Fmoc-Amino acid series;Protected Amino Acids;Fluorenes, Flurenones;AMINOACIDS DERIVATIVES;Amino Acid Derivatives;Amino Acids;Azepanes/Diazepanes
Mol File:29022-11-5.mol
Fmoc-Gly-OH Structure
Fmoc-Gly-OH Chemical Properties
Melting point 174-175 °C(lit.)
Boiling point 438.82°C (rough estimate)
density 1.1671 (rough estimate)
refractive index 1.4500 (estimate)
storage temp. 2-8°C
solubility almost transparency in Methanol
pka3.89±0.10(Predicted)
form Powder
color White
BRN 2163967
Major Applicationpeptide synthesis
InChIInChI=1S/C17H15NO4/c19-16(20)9-18-17(21)22-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15H,9-10H2,(H,18,21)(H,19,20)
InChIKeyNDKDFTQNXLHCGO-UHFFFAOYSA-N
SMILESC(O)(=O)CNC(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)=O
CAS DataBase Reference29022-11-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 24/25-36-26
WGK Germany 3
HS Code 29242995
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
Fmoc-Gly-OH English
ACROS English
SigmaAldrich English
ALFA English
Fmoc-Gly-OH Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
UsesFmoc-Gly-OH is an N-Fmoc-protected form of Glycine (G615990). Glycine is a nonessential amino acid that acts as an inhibitory neyrotransmitter in the vertebrate central nervous system. Glycine also posesses cytoprotective against oxidant damage in the kidney.
PreparationGlycine (Gly) (0.5 g, 6.66 mmol) was dissolved in 10% NaCO3 (14 ml) under stirring in a 50-ml flask. To the resulting solution, which had been put into an ice bath, 9-fluorenylmethoxycarbonyl chloride (Fmoc-Cl) (1.72 g, 6.66 mmol) in dioxane (12 ml) was gradually added. The reaction mixture was stirred at room temperature for 4 hours. Then added water (150 ml) to the mixture. The aqueous phase layer was separated from the reaction mixture and stripped with ether three times (75 ml×3). The stripped aqueous layer was acidified with 2N HCl aqueous solution to a pH=2, followed by extraction with ethyl acetate three times (75 ml×3). The organic phase layer was recovered and concentrated to obtain crude product of 1.70 g. The crude product was recrystallized in a mixed solvent of ethyl acetate hexane=1:2 (30 ml), and white solid denoted as Fmoc-Gly-OH was obtained after filtration at a reduced pressure.
Fmoc-Gly-OH
General Description Fmoc-Gly-OH is used for fmoc solid-phase peptide synthesis.
reaction suitabilityreaction type: Fmoc solid-phase peptide synthesis
Tag:Fmoc-Gly-OH(29022-11-5) Related Product Information
9-Fluorenylmethyl chloroformate 4-Aminophenylacetic acid N-Carbobenzyloxyglycine 4-Hydroxy-D-(-)-2-phenylglycine Glycine Fmoc-Aib-OH Fmoc-OSu Fmoc-Lys(Boc)-OH FMOC-O-tert-Butyl-L-serine Fmoc-Leu-OH Fmoc-Tyr(tBu)-OH FMOC-AMINOXYACETIC ACID Fmoc-L-Serine 2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-butanoic acid FMOC-N-METHYL-TRANEXAMIC ACID Fmoc-L-Tyr(propargyl)-OH Fmoc-Asn(Trt)-OH FMOC-TRANEXAMIC ACID

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