ChemicalBook--->CAS DataBase List--->28320-73-2

28320-73-2

28320-73-2 Structure

28320-73-2 Structure
IdentificationBack Directory
[Name]

BOC-GLY-GLY-GLY-OH
[CAS]

28320-73-2
[Synonyms]

Boc-GGG-OH
BOC-(GLY)3-OH
Boc-Gly-Gly-Gly
BOC-GLY-GLY-GLY-OH
N-Boc-glycylglycylglycine
BOC-L-GLYCYL GLYCYL GLYCINE
REF DUPL: Boc-Gly-Gly-Gly-OH
Boc-Gly-Gly-Gly-OH≥ 97.5% (HPLC)
(Tert-Butoxy)Carbonyl Gly-Gly-Gly-OH
(tert-Butoxycarbonyl)glycylglycylglycine
Nα-t-Butoxycarbonyl-glycyl-glycyl-glycine
N-ALPHA-T-BUTOXYCARBONYL-GLYCYL-GLYCYL-GLYCINE
N-[N-[N-[(tert-Butoxyl)carbonyl]glycyl]glycyl]glycine
Glycine, N-[(1,1-dimethylethoxy)carbonyl]glycylglycyl-
N-[N-(N-Carboxyglycyl)glycyl]glycine N-tert-butyl ester
2,2-dimethyl-4,7,10-trioxo-3-oxa-5,8,11-triazatridecan-13-oic acid
2-[2-(2-{[(tert-butoxy)carbonyl]amino}acetamido)acetamido]acetic acid
2-[[2-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]acetyl]amino]acetyl]amino]acetic acid
[Molecular Formula]

C11H19N3O6
[MDL Number]

MFCD00190687
[MOL File]

28320-73-2.mol
[Molecular Weight]

289.29
Chemical PropertiesBack Directory
[Melting point ]

205 °C
[Boiling point ]

641.8±50.0 °C(Predicted)
[density ]

1.263
[storage temp. ]

Sealed in dry,2-8°C
[form ]

Solid
[pka]

3.33±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2924297099
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

Boc-Gly-Gly-Gly-OH is used in synthesis method for terlipressin.
[Synthesis]

Glycyl-glycyl-glycine

556-33-2

Di-tert-butyl dicarbonate

24424-99-5

BOC-GLY-GLY-GLY-OH

28320-73-2

GENERAL METHOD: Glycyl-glycyl-glycine (1 mmol) was slowly added to a solution of ethanol (1 mL) containing guanidine hydrochloride (15 mmol) and di-tert-butyl dicarbonate (2.5-3 mmol) under stirring conditions, and the reaction temperature was maintained at 35-40°C. The reaction mixture was stirred continuously until a clarified solution was formed. Subsequently, the ethanol was removed by evaporation under vacuum. The residue was washed sequentially with distilled water (2 mL) and hexane or petroleum ether (2 mL) to obtain almost pure Boc-glycine-glycine-glycine. The crude product can be recrystallized if further improvement of product purity is required.

[References]

[1] European Journal of Organic Chemistry, 2017, vol. 2017, # 41, p. 6209 - 6227
[2] Carbohydrate Research, 2006, vol. 341, # 10, p. 1657 - 1668
[3] Tetrahedron Letters, 2011, vol. 52, # 12, p. 1260 - 1264
[4] Organic and Biomolecular Chemistry, 2006, vol. 4, # 19, p. 3626 - 3638
[5] Tetrahedron Letters, 2000, vol. 41, # 18, p. 3433 - 3436
Spectrum DetailBack Directory
[Spectrum Detail]

BOC-GLY-GLY-GLY-OH(28320-73-2)1HNMR
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