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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)-

(2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid

O=C(OC(C)(C)C)NC(C(=O)O)C(C)C Request for Quotation
Chemical Name: (2S)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid
CAS Number: 54895-12-4
Product Number: AG0039HY(AGN-PC-00DAIM)
Synonyms:
MDL No: MFCD00069973
Molecular Formula: C10H19NO4
Molecular Weight: 217.2622

Identification/Properties

Computed Properties
Molecular Weight:
217.265g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
217.131g/mol
Monoisotopic Mass:
217.131g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
242
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
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


Boc-DL-Valine, also known as N-tert-butoxycarbonyl-DL-valine, is a versatile compound commonly used in chemical synthesis processes. Its primary application lies in the field of peptide synthesis, where it serves as a key building block for constructing peptides with specific sequences and structures. In peptide synthesis, Boc-DL-Valine acts as a protected amino acid derivative, allowing chemists to selectively add it to the peptide chain without interference from other reactive functional groups. By incorporating Boc-DL-Valine at desired positions within the peptide sequence, researchers can precisely control the overall structure and properties of the synthesized peptide.Moreover, Boc-DL-Valine's tert-butoxycarbonyl (Boc) protecting group provides stability to the amino acid, preventing undesired reactions during the synthesis process. This protective group can be easily removed under mild conditions, exposing the free amino group of valine for further reaction steps, such as peptide coupling or deprotection.Overall, Boc-DL-Valine plays a vital role in the efficient and selective synthesis of complex peptides, making it an indispensable tool for chemical researchers and drug development professionals working in the field of biochemistry and pharmaceuticals.