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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-Valine

N[C@H](C(=O)O)C(C)C Request for Quotation
Chemical Name: L-Valine
CAS Number: 516-06-3
Product Number: AG00I988(AGN-PC-0OBJHO)
Synonyms:
MDL No:
Molecular Formula: C5H11NO2
Molecular Weight: 117.14634

Identification/Properties

Properties
MP:
283.5 - 285 °C
BP:
213.642 °C at 760 mmHg
Storage:
Light sensitive;Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.4650 (estimate)
Computed Properties
Molecular Weight:
117.148g/mol
XLogP3:
-2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
117.079g/mol
Monoisotopic Mass:
117.079g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
90.4
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


DL-Valine, also known as DL-2-Amino-3-methylbutanoic acid, is a non-essential amino acid that plays a crucial role in chemical synthesis. This versatile compound is commonly utilized in the production of pharmaceuticals, food additives, and specialty chemicals. In chemical synthesis, DL-Valine acts as a building block for creating various compounds due to its unique structural properties and reactivity.One key application of DL-Valine in chemical synthesis is in peptide synthesis. As an essential component of proteins, DL-Valine is often used to construct peptide chains through solid-phase peptide synthesis (SPPS) or liquid-phase peptide synthesis (LPPS). By incorporating DL-Valine into the peptide sequence, chemists can tailor the properties and functions of the resulting peptides for specific applications in drug discovery, biotechnology, and materials science.Additionally, DL-Valine is a precursor in the synthesis of pharmaceuticals such as antiviral drugs, anticancer agents, and antibiotics. Its ability to participate in various chemical reactions, including condensation, reduction, and enzymatic transformations, makes it a valuable building block for creating bioactive molecules with diverse pharmacological activities.Furthermore, DL-Valine finds applications in the manufacturing of flavor enhancers, nutritional supplements, and specialty chemicals. Its role as a chiral entity allows for the production of enantiopure compounds, which are essential for industries requiring high purity and specific stereochemistry in their products.Overall, DL-Valine's versatility and reactivity make it a valuable asset in chemical synthesis, enabling the creation of a wide range of compounds with diverse applications in the pharmaceutical, food, and chemical industries.