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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)-

H-Met-OMe• HCl

CSCC[C@@H](C(=O)OC)N Request for Quotation
Chemical Name: H-Met-OMe• HCl
CAS Number: 2491-18-1
Product Number: AG00I4RF(AGN-PC-0WADGP)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
151-153 °C(lit.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Hygroscopic
Refractive Index:
26 ° (C=1, H2O)
Computed Properties
Molecular Weight:
199.693g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
199.043g/mol
Monoisotopic Mass:
199.043g/mol
Topological Polar Surface Area:
77.6A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
108
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


H-Met-OMe.HCl, or hydroxymethyl metaraminol hydrochloride, is a valuable chemical reagent used in organic synthesis for the protection of amino groups. By selectively blocking the amino functionality of molecules with this reagent, chemists are able to control the course of a reaction and protect sensitive functional groups during various synthetic procedures. This protective group strategy enables the synthesis of complex compounds by preventing unwanted reactions at specific sites within a molecule. H-Met-OMe.HCl is commonly employed in peptide chemistry, pharmaceutical development, and organic synthesis methodologies requiring precise amino group manipulation. Its application in chemical synthesis highlights its crucial role as a versatile and reliable tool in the hands of synthetic chemists.