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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)-

Glycine, phenylmethyl ester, 4-methylbenzenesulfonate

Cc1ccc(cc1)S(=O)(=O)O.NCC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: Glycine, phenylmethyl ester, 4-methylbenzenesulfonate
CAS Number: 1738-76-7
Product Number: AG001Z72(AGN-PC-0QAFCQ)
Synonyms:
MDL No:
Molecular Formula: C16H19NO5S
Molecular Weight: 337.3908

Identification/Properties

Properties
MP:
132-134 °C
BP:
245.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Solubility:
methanol: 0.1 g/mL, clear
Computed Properties
Molecular Weight:
337.39g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
337.098g/mol
Monoisotopic Mass:
337.098g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
348
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


H-Gly-OBzl.TosOH, also known as N-(tert-butoxycarbonyl)-L-histidine benzyl ester and tosylate, is a versatile compound commonly utilized in organic synthesis for its unique reactivity and functionality. This compound serves as a crucial intermediate in the preparation of various bioactive molecules, pharmaceuticals, and peptide synthesis.In chemical synthesis, H-Gly-OBzl.TosOH acts as a protecting group for the amino acid histidine. By strategically masking the reactive groups of histidine, this compound helps to prevent unwanted side reactions during the synthesis of complex molecules. Furthermore, the tosyl group attached to the molecule provides an additional handle for selective deprotection and functional group manipulation.Overall, H-Gly-OBzl.TosOH plays a pivotal role in the efficient and precise synthesis of diverse organic compounds by facilitating the controlled manipulation of functional groups and protecting key reactive sites. Its versatility and reliability make it a valuable tool for chemists working in medicinal chemistry, peptide synthesis, and other fields requiring the precise control of chemical reactions.