1. Home
  2. L-Valine, L-alanyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, L-alanyl-

C[C@@H](C(=O)N[C@H](C(=O)O)C(C)C)N Request for Quotation
Chemical Name: L-Valine, L-alanyl-
CAS Number: 1999-46-8
Product Number: AG002CG8(AGN-PC-0O6YV8)
Synonyms:
MDL No:
Molecular Formula: C8H16N2O3
Molecular Weight: 188.2242

Identification/Properties

Properties
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
188.227g/mol
XLogP3:
-3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
188.116g/mol
Monoisotopic Mass:
188.116g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
204
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(2-Aminopropanamido)-3-methylbutanoic acid, commonly known as $name$, is a versatile compound that finds wide applications in chemical synthesis. This compound serves as a crucial building block in organic chemistry, owing to its unique structure and reactivity. In chemical synthesis, $name$ is commonly used as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features make it an ideal precursor for the synthesis of complex molecules, allowing chemists to efficiently access a wide range of target compounds. With its ability to participate in various chemical reactions, $name$ plays a pivotal role in the development of novel materials and compounds with diverse functionalities. Its versatile nature and strategic position in synthetic pathways make it a valuable tool for chemists seeking to explore new frontiers in organic chemistry.