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60421-20-7

60421-20-7 Structure

60421-20-7 Structure
IdentificationBack Directory
[Name]

H-Aib-OBzl
[CAS]

60421-20-7
[Synonyms]

aib-obzl.hcl
H-Aib-Obn.HCl
H-Aib-OBzl USP/EP/BP
Benzyl 2-amino-2-methylpropanoate HCl
Benzyl α-aminoisobutyrate hydrochloride
Benzyl α-aminoisobutyrate hydrochloride
2-Methylalanine benzyl ester hydrochloride
Benzyl alpha-aMinoisobutyrate hydrochloride
Benzyl 2-amino-2-methylpropionate hydrochloride
2-Aminoisobutyric acid benzyl ester hydrochloride
2-AMino-2-Methylpropanoic acid benzyl ester HCl salt
alpha-Aminoisobutyric acid benzyl ester hydrochloride
Alanine, 2-methyl-, phenylmethyl ester, hydrochloride
2-Amino-2-methylpropionic acid benzyl ester hydrochloride
[Molecular Formula]

C11H16ClNO2
[MDL Number]

MFCD14155677
[MOL File]

60421-20-7.mol
[Molecular Weight]

229.703
Chemical PropertiesBack Directory
[Melting point ]

170-171℃
[storage temp. ]

2-8°C
[solubility ]

H2O: soluble50mg/mL, clear, colorless
[form ]

powder
[Appearance]

White to off-white Solid
[Water Solubility ]

H2O: 50mg/mL, clear, colorless
[BRN ]

5149947
[Major Application]

peptide synthesis
[InChI]

InChI=1S/C11H15NO2.ClH/c1-11(2,12)10(13)14-8-9-6-4-3-5-7-9;/h3-7H,8,12H2,1-2H3;1H
[InChIKey]

OXUUEIDXKLFLER-UHFFFAOYSA-N
[SMILES]

C(OCC1=CC=CC=C1)(=O)C(N)(C)C.[H]Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H317-H319
[Precautionary statements ]

P280-P305+P351+P338
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

Benzyl 2-amino-2-methylpropanoate hydrochloride, also known as H-Aib-OBzl, is a white solid.
[Uses]

peptide synthesis
[Preparation]

A mixture of 2-amino-2- methylpropanoic acid (3 g, 29.1 mmol), benzyl alcohol (12 mL, 115 mmol), and p- toluenesulfonic acid monohydrate (5.53 g, 29.1 mmol) in toluene (40 mL) was heated under reflux overnight. Additional benzyl alcohol (12 mL, 115 mmol) was added and the reaction mixture was heated with a Dean Starck overnight. The reaction mixture was concentrated under reduced pressure and washed with diethyl ether. Diethyl ether was removed, and then the residue was dissolved in ethyl acetate and washed with a saturated aqueous NaHC03 solution. The organic layer was dried over Na2S04 and concentrated under reduced pressure. The resulting product was triturated with diethyl ether and HCI in dioxane. The solid was filtered, washed with diethyl ether and dried under reduced pressure to afford benzyl 2-amino-2-methylpropanoate hydrochloride.
H-Aib-OBzl
[reaction suitability]

reaction type: solution phase peptide synthesis
[Waste Disposal]

The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Spectrum DetailBack Directory
[Spectrum Detail]

H-Aib-OBzl(60421-20-7)1HNMR
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