1. Home
  2. D-Valine, 3-methyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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, 3-methyl-

N[C@H](C(C)(C)C)C(=O)O Request for Quotation
Chemical Name: D-Valine, 3-methyl-
CAS Number: 26782-71-8
Product Number: AG003PWA(AGN-PC-0O8GA4)
Synonyms:
MDL No: MFCD00004265
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729

Identification/Properties

Properties
MP:
≥300 °C(lit.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
9 ° (C=3, H2O)
Computed Properties
Molecular Weight:
131.175g/mol
XLogP3:
-1.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
131.095g/mol
Monoisotopic Mass:
131.095g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
115
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-Methyl-D-valine is a versatile compound widely utilized in chemical synthesis due to its unique structural features and reactivity. Its application in the field of organic chemistry includes serving as a chiral building block for the preparation of biologically active molecules, pharmaceutical intermediates, and complex natural products. In asymmetric synthesis, 3-Methyl-D-valine plays a key role in creating stereochemically pure compounds, making it an essential tool for the development of new drugs and materials with enhanced properties. Additionally, this compound is utilized in the production of peptide-based materials and as a precursor in the synthesis of peptide nucleic acids. Its ability to impart chirality and enhance molecular complexity makes 3-Methyl-D-valine a valuable component in modern chemical research and development.