CAS 839710-38-2
:(S)-N-Boc-3-morpholineacetic acid
Description:
(S)-N-Boc-3-morpholineacetic acid is a chemical compound characterized by its chiral structure, which includes a morpholine ring and a Boc (tert-butyloxycarbonyl) protecting group. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The presence of the morpholine moiety contributes to its potential as a building block in medicinal chemistry, offering properties such as improved solubility and bioavailability. The Boc group serves as a protective group for the amine, allowing for selective reactions without affecting the amine functionality. This compound is generally solid at room temperature and is soluble in polar organic solvents. Its chirality is significant in biological applications, as the (S) configuration may influence the compound's interaction with biological targets. Safety and handling precautions should be observed, as with many chemical substances, to mitigate any potential hazards associated with its use.
Formula:C11H19NO5
InChI:InChI=1/C11H19NO5/c1-11(2,3)17-10(15)12-4-5-16-7-8(12)6-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m0/s1
InChI key:QVOPNRRQHPWQMF-QMMMGPOBSA-N
SMILES:CC(C)(C)OC(=O)N1CCOC[C@@H]1CC(=O)O
Synonyms:- [(3S)-4-(tert-Butoxycarbonyl)morpholin-3-yl]acetic acid
- 3-morpholineacetic acid, 4-[(1,1-dimethylethoxy)carbonyl]-, (3S)-
- (S)-4-Boc-3-Morpholineacetic Acid
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(S)-2-(4-(tert-Butoxycarbonyl)morpholin-3-yl)acetic acid
CAS:(S)-2-(4-(tert-Butoxycarbonyl)morpholin-3-yl)acetic acidFormula:C11H19NO5Purity:0.97Molecular weight:245.27(S)-2-(4-(tert-Butoxycarbonyl)morpholin-3-yl)acetic acid
CAS:Formula:C11H19NO5Purity:97%Color and Shape:SolidMolecular weight:245.2723(S)-2-(4-(tert-Butoxycarbonyl)morpholin-3-yl)acetic acid
CAS:(S)-2-(4-(tert-Butoxycarbonyl)morpholin-3-yl)acetic acidFormula:C11H19NO5Purity:97%Molecular weight:245.27



