Benzyl N-[(1R)-1-[Methoxy(methyl)carbamoyl]ethyl]carbamate - CAS 152169-60-3
Catalog: |
BB072667 |
Product Name: |
Benzyl N-[(1R)-1-[Methoxy(methyl)carbamoyl]ethyl]carbamate |
CAS: |
152169-60-3 |
Synonyms: |
benzyl N-[(1R)-1-[methoxy(methyl)carbamoyl]ethyl]carbamate; (R)-Benzyl (1-(methoxy(methyl)amino)-1-oxopropan-2-yl)carbamate; benzyl n-((1r)-1-(methoxy(methyl)carbamoyl)ethyl)carbamate |
IUPAC Name: | benzyl N-[(2R)-1-[methoxy(methyl)amino]-1-oxopropan-2-yl]carbamate |
Description: | Benzyl N-[(1R)-1-[Methoxy(methyl)carbamoyl]ethyl]carbamate is an intermediate in the synthesis of (R)-1,1-Diethoxy-2-propanamine (D442115), which can be used for the synthesis of N-protected a-amino aldehydes occur as C-terminal units of peptide aldehydes with enzyme inhibitor activity, such as Leupeptin. They can also be used for the preparation of amino sugars, and unusual amino acids. |
Molecular Weight: | 266.29 |
Molecular Formula: | C13H18N2O4 |
Canonical SMILES: | CC(C(=O)N(C)OC)NC(=O)OCC1=CC=CC=C1 |
InChI: | InChI=1S/C13H18N2O4/c1-10(12(16)15(2)18-3)14-13(17)19-9-11-7-5-4-6-8-11/h4-8,10H,9H2,1-3H3,(H,14,17)/t10-/m1/s1 |
InChI Key: | JJWLCBIYQXRMNO-SNVBAGLBSA-N |
Solubility: | Chloroform |
Appearance: | White Solid |
References: | Bringmann, G., et al. J. Synthesis, 608 (1989); Guillaumie, F., Tetrahedron Letters, 41, 6131 (200). |
Complexity: | 303 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 266.12665706 |
Formal Charge: | 0 |
Heavy Atom Count: | 19 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 266.12665706 |
Rotatable Bond Count: | 6 |
Topological Polar Surface Area: | 67.9Ų |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.4 |
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