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Boc-Ala-OH

Catalog Number
ACM15761383
Product Name
Boc-Ala-OH
Structure
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CAS
15761-38-3
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Synonyms
CS-W009232; (2S)-2-[(tert-butoxy)carbonylamino]propanoic acid; t-butyloxycarbonylalanine; N-tertiarybutoxycarbonyl-L-alanine; t-Boc-Ala; J-300002; N-t-butoxycarbonyl-L-alanine; AB1002648; alanine, N-[(1,1-dimethylethoxy)carbonyl]-; AKOS015924055;
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid;
Molecular Weight
189.211g/mol
Molecular Formula
C8H15NO4;
Canonical SMILES
CC(C(=O)O)NC(=O)OC(C)(C)C;
InChI
InChI=1S/C8H15NO4/c1-5(6(10)11)9-7(12)13-8(2,3)4/h5H,1-4H3,(H,9,12)(H,10,11)/t5-/m0/s1;
InChI Key
QVHJQCGUWFKTSE-YFKPBYRVSA-N;
Storage
−20°C
Complexity
207
Covalently-Bonded Unit Count
1
Defined Atom Stereocenter Count
1
EC Number
239-847-8
Exact Mass
189.1g/mol
H-Bond Acceptor
4
H-Bond Donor
2
Heavy Atom Count
13
Monoisotopic Mass
189.1g/mol
Rotatable Bond Count
4
Topological Polar Surface Area
75.6A^2
UNII
VBSZA1BT4G
Application
Boc-Ala-OH is a versatile reagent that plays a crucial role in various chemical syntheses. As a white to off-white microcrystalline powder, it is employed in the preparation of N-propargylalanine, which is an essential precursor for generating N-(3-aryl)propylated alanine residues. Additionally, Boc-Ala-OH is instrumental in resolving racemic mixtures of compounds such as 3,3'-bis(benzyloxy)-1,1'-binaphthalene-2,2'-diol. It also facilitates the one-pot synthesis of hybrid tripeptidomimetics that include both amide and imide functionalities, showcasing its utility in creating complex molecular structures.
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