Butanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-,phenylmethyl ester, (3R)-


Chemical Name: Butanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxy-,phenylmethyl ester, (3R)-
CAS Number: 182748-72-7
Product Number: AG00243R(AGN-PC-0QC9VR)
Synonyms:
MDL No:
Molecular Formula: C16H23NO5
Molecular Weight: 309.3575

Identification/Properties


Properties
BP:
467.4±45.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
309.362g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
9
Exact Mass:
309.158g/mol
Monoisotopic Mass:
309.158g/mol
Topological Polar Surface Area:
84.9A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
358
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Boc-D-aspartinol 4-Benzyl Ester is a key compound used in chemical synthesis for the selective protection of amino groups. This derivative is particularly valuable in peptide synthesis and organic chemistry reactions where the temporary protection of specific functional groups is required to prevent unwanted side reactions. By incorporating Boc-D-aspartinol 4-Benzyl Ester into a synthetic strategy, chemists can control the reaction pathway, ensuring the desired product is formed efficiently and with high purity. This compound's strategic use in chemical synthesis highlights its importance as a versatile tool for researchers and practitioners in the field.