CAS 132286-77-2
:BOC-ASP(OALL)-OH
Description:
BOC-ASP(OALL)-OH, with the CAS number 132286-77-2, is a chemical compound that features a protected form of aspartic acid. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, which is commonly used in peptide synthesis to prevent unwanted reactions. The "ASP" indicates the presence of aspartic acid, an amino acid that plays a crucial role in protein synthesis and metabolism. The "OALL" portion suggests the presence of an allyl group, which can be involved in further chemical transformations or reactions. The hydroxyl (-OH) group indicates that the compound is likely to be a carboxylic acid derivative, contributing to its reactivity and potential applications in organic synthesis. Overall, BOC-ASP(OALL)-OH is utilized primarily in the field of medicinal chemistry and peptide synthesis, where the protection and selective reactivity of functional groups are essential for constructing complex molecules.
Formula:C12H19NO6
InChI:InChI=1/C12H19NO6/c1-5-6-18-9(14)7-8(10(15)16)13-11(17)19-12(2,3)4/h5,8H,1,6-7H2,2-4H3,(H,13,17)(H,15,16)/t8-/m0/s1
SMILES:C=CCOC(=O)C[C@@H](C(=O)O)N=C(O)OC(C)(C)C
Synonyms:- L-Aspartic Acid, N-[(1,1-Dimethylethoxy)Carbonyl]-, 4-(2-Propenyl) Ester
- (2S)-4-allyloxy-2-(tert-butoxycarbonylamino)-4-oxo-butanoic acid
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Found 4 products.
L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 4-(2-propen-1-yl) ester
CAS:Formula:C12H19NO6Purity:98%Color and Shape:SolidMolecular weight:273.2824Boc-asp(oall)-oh
CAS:Boc-asp(oall)-ohFormula:C12H19NO6Purity:97%Color and Shape: yellow solidMolecular weight:273.28g/molBoc-L-aspartic acid-b-allyl ester
CAS:Formula:C12H19NO6Purity:98%Color and Shape:SolidMolecular weight:273.285



