1. Home
  2. D-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl)ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

D-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl)ester

OC(=O)C[C@H](C(=O)OC(C)(C)C)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: D-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(1,1-dimethylethyl)ester
CAS Number: 77004-75-2
Product Number: AG003C9Y(AGN-PC-0UAWAK)
Synonyms:
MDL No: MFCD00236827
Molecular Formula: C13H23NO6
Molecular Weight: 289.3248

Identification/Properties

Properties
BP:
429°C at 760 mmHg
Storage:
Keep in dry area;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
289.328g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
289.153g/mol
Monoisotopic Mass:
289.153g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
377
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The (R)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid, also known as $name$, is a valuable compound in chemical synthesis owing to its versatile applications. It serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, (R)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is widely utilized as a chiral building block due to its unique stereochemistry. Its presence can impart optical activity in target molecules, making it essential in the preparation of enantiomerically pure compounds. Furthermore, its tert-butoxy and tert-butoxycarbonyl functionalities provide opportunities for selective derivatization and functional group transformations during synthetic routes. This compound plays a crucial role in peptide and amino acid synthesis, where its amino and carboxylic acid moieties participate in peptide bond formation reactions. By incorporating (R)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid into peptide sequences, chemists can control the peptide's chirality and structure, ultimately influencing its biological activity and properties. Overall, (R)-4-(tert-Butoxy)-3-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid is a valuable tool in modern chemical synthesis, enabling the construction of complex molecules with precision and efficiency. Its diverse applications across various fields make it indispensable for researchers and scientists striving to develop new and innovative compounds.