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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-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-, compd. withN-cyclohexylcyclohexanamine (1:1)

C1CCC(CC1)NC1CCCCC1.CN([C@H](C(=O)O)Cc1ccc(cc1)O)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: L-Tyrosine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-, compd. withN-cyclohexylcyclohexanamine (1:1)
CAS Number: 95105-25-2
Product Number: AG003OHX(AGN-PC-0W4Q2N)
Synonyms:
MDL No:
Molecular Formula: C27H44N2O5
Molecular Weight: 476.6487

Identification/Properties

Properties
BP:
626.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
476.658g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
8
Exact Mass:
476.325g/mol
Monoisotopic Mass:
476.325g/mol
Topological Polar Surface Area:
99.1A^2
Heavy Atom Count:
34
Formal Charge:
0
Complexity:
485
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-N-Me-Tyr-OH.DCHA is a useful compound in chemical synthesis, specifically in peptide and drug development. Its application lies in the protection of the amino group of tyrosine residues during peptide synthesis, allowing for selective deprotection under mild conditions to reveal the free amino group for further coupling reactions. This controlled protection strategy is crucial in the stepwise assembly of complex peptides and pharmaceuticals, enabling precise control over the synthesis process and ensuring the desired product is obtained. Boc-N-Me-Tyr-OH.DCHA plays a critical role in enhancing the efficiency and success of peptide synthesis procedures, making it an essential tool for chemists working in the field of drug discovery and development.