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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)-

D-Valine, phenylmethyl ester, 4-methylbenzenesulfonate

N[C@@H](C(=O)OCc1ccccc1)C(C)C.Cc1ccc(cc1)S(=O)(=O)O Request for Quotation
Chemical Name: D-Valine, phenylmethyl ester, 4-methylbenzenesulfonate
CAS Number: 17662-84-9
Product Number: AG0024SB(AGN-PC-0QAYMK)
Synonyms:
MDL No:
Molecular Formula: C19H25NO5S
Molecular Weight: 379.4705

Identification/Properties

Properties
MP:
162 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
4 ° (C=3.2, MeOH)
Computed Properties
Molecular Weight:
379.471g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
6
Exact Mass:
379.145g/mol
Monoisotopic Mass:
379.145g/mol
Topological Polar Surface Area:
115A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
404
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


When it comes to chemical synthesis processes, H-D-Val-Obzl.TosOH plays a crucial role as a versatile reagent. Widely utilized in the realm of organic chemistry, this compound is valued for its ability to facilitate various reactions with precision and efficiency. Specifically, H-D-Val-Obzl.TosOH is frequently employed as a key building block in peptide synthesis, enabling the creation of complex peptide structures with high purity and yield. Its strategic use in peptide bond formation and protection makes it an indispensable tool for chemists aiming to synthesize biologically active peptides or conduct research in the field of pharmaceuticals. Beyond peptide synthesis, H-D-Val-Obzl.TosOH demonstrates utility in the creation of diverse organic molecules and pharmaceutical intermediates, showcasing its versatility and significance in advancing chemical synthesis methodologies.