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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)-

Valine, 1,1-dimethylethyl ester, hydrochloride

CC([C@@H](C(=O)OC(C)(C)C)N)C.Cl Request for Quotation
Chemical Name: Valine, 1,1-dimethylethyl ester, hydrochloride
CAS Number: 13518-40-6
Product Number: AG003546(AGN-PC-0O17I4)
Synonyms:
MDL No: MFCD00034863
Molecular Formula: C9H20ClNO2
Molecular Weight: 209.7136

Identification/Properties

Properties
MP:
142.0 to 146.0 °C
BP:
241.7 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
209.714g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
209.118g/mol
Monoisotopic Mass:
209.118g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
158
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-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


L-Valine tert-butyl ester hydrochloride, a versatile compound utilized in chemical synthesis, demonstrates a wide range of applications in organic chemistry. As a derivative of the amino acid L-Valine, this compound plays a crucial role in the preparation of various pharmaceuticals and organic compounds. Its unique structure and reactivity make it an essential building block for the synthesis of peptides, pharmaceuticals, and other complex organic molecules. With its tert-butyl ester group, L-Valine tert-butyl ester hydrochloride offers increased stability and protection of the amino acid functionality during synthetic transformations. Whether used as a protecting group or a key intermediate, this compound proves to be valuable in the intricate processes of chemical synthesis, enabling the efficient construction of diverse organic structures.