Fmoc-Gly-OH

Fmoc-Gly-OH Basic information
Product Name:Fmoc-Gly-OH
Synonyms:9-FLUORENYLMETHOXYCARBONYL-GLYCINE;FMOC-GLYCINE;F-FMOC-GLYCINE;N-alpha-(9-fluorenylmethyloxycarbonyl)-L-glycine;FMOC-Glycine,98%;Fmoc-glycine N-(9-Fluorenylmethoxycarbonyl)-glycine;N-Fmoc-glycine Fmoc-Gly-OH;FMoc-Gly-OH >=98.0% (T)
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
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
MSDS Information
ProviderLanguage
Fmoc-Gly-OH English
SigmaAldrich English
ACROS 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 DescriptionThe product number for this product was previously 04-12-1001.

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Fmoc-Gly-OH Preparation Products And Raw materials
Preparation ProductsPiperidine, 1-(9H-fluoren-9-ylmethyl)--->FMOC-ALA-GLY-OH-->FMOC-GLY-OSU-->FMOC-GLY-OPFP-->MELITTIN-->5-Bromo-7-nitroindoline-->FMOC-SARCOSINE MONOHYDRATE-->N-Fmoc-(1-benzotriazolylcarbonyl)methylamine-->Copper Peptide-->Fmoc-Gly-DL-Ala-->H-HIS-GLY-GLY-OH-->methyl 2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)acetate-->Fmoc-Gly-ODhbt
FMOC-Ala-OH fmoc-glycine N-carboxy anhydride,FMOC-GLYCINE-NCA FMOC-ASP(OTBU)-OPFP Fmoc-glycine Sasrin(R) resin ester,FMOC-GLYCINE-SASRIN(TM)-RESIN,N-FMOC-GLYCINE SASRIN RESIN ESTER FMOC-GLYCINE-HMPB-4-ME-BENZHYDRYLAM. P.& N-FMOC-GLYCINE, [1-14C] N-ALPHA-FMOC-GLYCINE-ETHYLAMIDE-SIEBER RESIN Fmoc-Aib-OH GlycineMax FMOC-GLYCINE, POLYMER-BOUND ON WANG RESI,FMOC-GLYCINE POLYMER-BOUND ON WANG FMOC-GLYCINE, POLYMER-BOUND ON WANG RESIN FMOC-GLYCINE 4-BENZYLOXYBENZYL ESTER N-FMOC-(GLYCINE-UL-14C) N-FMOC-GLYCINE, [14C(U)]- Fmoc-glycine 4-[poly(oxyethylene)carbamoyl]trityl ester polymer-bound FMOC-NLE-OH N-ALPHA-FMOC-GLYCINE-METHYLAMIDE-SIEBER RESIN Fmoc

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