1. Home
  2. Carbamic acid,[(1S)-4-amino-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-4-oxobutyl]-,1,1-dimethylethyl ester

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Carbamic acid,[(1S)-4-amino-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-4-oxobutyl]-,1,1-dimethylethyl ester

O=C([C@@H](NC(=O)OC(C)(C)C)CCC(=O)N)ON1C(=O)CCC1=O Request for Quotation
Chemical Name: Carbamic acid,[(1S)-4-amino-1-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]-4-oxobutyl]-,1,1-dimethylethyl ester
CAS Number: 18800-78-7
Product Number: AG002GN6(AGN-PC-0QH4HV)
Synonyms:
MDL No:
Molecular Formula: C14H21N3O7
Molecular Weight: 343.3324

Identification/Properties

Computed Properties
Molecular Weight:
343.33g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
9
Exact Mass:
343.13795g/mol
Monoisotopic Mass:
343.13795g/mol
Topological Polar Surface Area:
145Ų
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
537
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


Boc-Gln-Osu, also known as Boc-Glutamine O-succinimide ester, is a key reagent widely used in chemical synthesis, particularly in peptide synthesis. This compound plays a crucial role as a protected amino acid derivative, facilitating the stepwise assembly of peptides with high purity and efficiency.In chemical synthesis, Boc-Gln-Osu is utilized as a building block for introducing glutamine residues into peptide chains. The Boc (tert-butoxycarbonyl) protecting group shields the amino group of glutamine, preventing undesired reactions at this site during the peptide coupling process. Additionally, the Osu (O-succinimide) ester moiety ensures efficient peptide bond formation by reacting selectively with amino groups under mild coupling conditions.Through its strategic incorporation into peptide synthesis protocols, Boc-Gln-Osu enables chemists to control the sequence and structure of peptides with precision. Its compatibility with standard peptide synthesis methodologies makes it a valuable tool for the production of peptides for various applications, including biochemical research, drug development, and more.