CAS 1334321-39-9
:(R)-N-Boc-3-Hydroxyadamantylglycine
Formule :C17H27NO5
InChI :InChI=1S/C17H27NO5/c1-15(2,3)23-14(21)18-12(13(19)20)16-5-10-4-11(6-16)8-17(22,7-10)9-16/h10-12,22H,4-9H2,1-3H3,(H,18,21)(H,19,20)/t10?,11?,12-,16?,17?/m0/s1
Code InChI :UKCKDSNFBFHSHC-JGCLWBMSSA-N
SMILES :CC(C)(C)OC(=O)N[C@@H](C(=O)O)C12CC3CC(C1)CC(C3)(C2)O
Trier par
Degré de pureté (%)
0
100
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0
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50
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90
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95
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100
6 produits trouvés.
(R)-N-Boc-3-hydroxyadaMantylglycine
CAS :(R)-N-Boc-3-hydroxyadaMantylglycineFormule :C17H27NO5Degré de pureté :95%Masse moléculaire :325.4(R)-N-Boc-3-hydroxyadaMantylglycine
CAS :Formule :C17H27NO5Degré de pureté :95%Couleur et forme :SolidMasse moléculaire :325.4000Saxagliptin Impurity 20
CAS :Formule :C17H27NO5Couleur et forme :White To Off-White SolidMasse moléculaire :325.41(2R)-2-((tert-Butoxycarbonyl)amino)-2-(3-hydroxyadamantan-1-yl)acetic acid
CAS :(2R)-2-((tert-Butoxycarbonyl)amino)-2-(3-hydroxyadamantan-1-yl)acetic acidFormule :C17H27NO5Degré de pureté :98%Masse moléculaire :325.4Boc-3-hydroxy-1-adamantyl-glycine
CAS :Boc-3-hydroxy-1-adamantyl-glycine is a catalytic, nucleophilic, chiral amino acid that is used in the synthesis of oximes. Boc-3-hydroxy-1-adamantyl-glycine has been shown to be an effective substitute for hydroxylamine in reductive amination reactions and can be used to synthesize some pharmaceuticals, including saxagliptin. This compound is stable under standard conditions and can be easily synthesized. It is also a powerful nucleophile that reacts with electrophiles such as chloroformates and sulfonyl chlorides.
Formule :C17H27NO5Degré de pureté :Min. 95%Masse moléculaire :325.4 g/mol
