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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-Tryptophan,1-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-, compd. withN-cyclohexylcyclohexanamine (1:1) (9CI)

C1CCC(CC1)NC1CCCCC1.O=C(N[C@H](C(=O)O)Cc1cn(c2c1cccc2)C(=O)OC(C)(C)C)OCc1ccccc1 Request for Quotation
Chemical Name: L-Tryptophan,1-[(1,1-dimethylethoxy)carbonyl]-N-[(phenylmethoxy)carbonyl]-, compd. withN-cyclohexylcyclohexanamine (1:1) (9CI)
CAS Number: 218938-57-9
Product Number: AG00C12E(AGN-PC-0QYE8W)
Synonyms:
MDL No:
Molecular Formula: C36H49N3O6
Molecular Weight: 619.7908

Identification/Properties

Computed Properties
Molecular Weight:
619.803g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
11
Exact Mass:
619.362g/mol
Monoisotopic Mass:
619.362g/mol
Topological Polar Surface Area:
119A^2
Heavy Atom Count:
45
Formal Charge:
0
Complexity:
786
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:
2
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

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Chemical Structure


The Z-Trp(Boc)-OH.DCHA compound is a versatile reagent commonly used in chemical synthesis for the protection of amino acids. It acts as a protecting group for the amino terminal of the amino acid tryptophan, protecting it from unwanted reactions during chemical transformations. This compound enables chemists to selectively modify other parts of the molecule without affecting the functionality of the tryptophan residue. By using Z-Trp(Boc)-OH.DCHA in their synthesis, researchers can control the sequence of reactions in complex organic synthesis processes, allowing for the creation of diverse molecules with specific properties and functions.