1. Home
  2. L-Leucine,N-benzoylglycyl-L-histidyl-, hydrate (9CI)

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)-

L-Leucine,N-benzoylglycyl-L-histidyl-, hydrate (9CI)

CC(C[C@@H](C(=O)O)NC(=O)[C@H](Cc1c[nH]cn1)NC(=O)CNC(=O)c1ccccc1)C.O Request for Quotation
Chemical Name: L-Leucine,N-benzoylglycyl-L-histidyl-, hydrate (9CI)
CAS Number: 207386-83-2
Product Number: AG002J08(AGN-PC-0QWH9C)
Synonyms:
MDL No:
Molecular Formula: C21H29N5O6
Molecular Weight: 447.4849

Identification/Properties

Computed Properties
Molecular Weight:
447.492g/mol
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
11
Exact Mass:
447.212g/mol
Monoisotopic Mass:
447.212g/mol
Topological Polar Surface Area:
154A^2
Heavy Atom Count:
32
Formal Charge:
0
Complexity:
636
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


N-Benzoyl-Gly-His-Leu xhydrate is commonly utilized in chemical synthesis as a key component for the preparation of peptide structures. This compound serves as a crucial building block in peptide synthesis due to its ability to facilitate the sequential addition of amino acid residues. By incorporating N-Benzoyl-Gly-His-Leu xhydrate into the synthesis process, researchers can efficiently create complex peptide sequences with high precision and purity. Its unique chemical properties enable precise control over the bonding and arrangement of amino acids, making it a valuable tool in the production of custom peptides for various research and pharmaceutical applications.