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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)-

CHEMBRDG-BB 4017705

COCCN(CC(=O)O)C Request for Quotation
Chemical Name: CHEMBRDG-BB 4017705
CAS Number: 915925-21-2
Product Number: AG00H1VR(AGN-PC-0WB7BW)
Synonyms:
MDL No:
Molecular Formula: C6H13NO3
Molecular Weight: 147.1723

Identification/Properties

Computed Properties
Molecular Weight:
147.174g/mol
XLogP3:
-2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
147.09g/mol
Monoisotopic Mass:
147.09g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
105
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-methoxyethyl)-N-methylglycine, also known as N-methoxyethylsarcosine, is a valuable compound in chemical synthesis due to its unique properties and versatile applications. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its incorporation into various synthetic routes enables the efficient production of complex molecules with enhanced bioactivity and chemical reactivity. Additionally, N-(2-methoxyethyl)-N-methylglycine plays a significant role in the development of novel materials and catalytic systems. Its structural flexibility and functional groups make it a crucial intermediate in the synthesis of diverse organic compounds. Furthermore, its compatibility with a wide range of reaction conditions makes it a versatile tool for chemists seeking to streamline synthetic processes and optimize product yields.