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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-Isoleucine, N-methyl-, methyl ester, hydrochloride

CN[C@H](C(=O)OC)[C@H](CC)C.Cl Request for Quotation
Chemical Name: L-Isoleucine, N-methyl-, methyl ester, hydrochloride
CAS Number: 3339-43-3
Product Number: AG00CHQT(AGN-PC-0O9114)
Synonyms:
MDL No:
Molecular Formula: C8H18ClNO2
Molecular Weight: 195.6870

Identification/Properties

Computed Properties
Molecular Weight:
195.687g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
195.103g/mol
Monoisotopic Mass:
195.103g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
125
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The N-ME-ILE-OME HCL is a versatile compound commonly used in chemical synthesis as a powerful reducing agent and organic intermediate. Its unique properties make it particularly useful for a wide range of applications in the laboratory setting. 
When used in chemical synthesis, N-ME-ILE-OME HCL functions as an efficient reagent for the reduction of various functional groups, such as ketones, aldehydes, and esters. This compound excels in facilitating complex transformations, making it an essential tool in organic chemistry. Its high reactivity and selectivity lead to precise control over reaction outcomes, enabling chemists to access important intermediates and final products with high yields and purity.
Additionally, N-ME-ILE-OME HCL serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its versatility and effectiveness in driving synthetic pathways make it an indispensable component in the development of new molecules with diverse applications. Chemists rely on the unique reactivity of N-ME-ILE-OME HCL to unlock innovative synthetic routes and streamline the production of valuable compounds in the field of chemical research and development.