Carbamic acid, [(1S,2S)-1-(hydroxymethyl)-2-(phenylmethoxy)propyl]-,1,1-dimethylethyl ester


Chemical Name: Carbamic acid, [(1S,2S)-1-(hydroxymethyl)-2-(phenylmethoxy)propyl]-,1,1-dimethylethyl ester
CAS Number: 168034-31-9
Product Number: AG001XQV(AGN-PC-0Q969W)
Synonyms:
MDL No:
Molecular Formula: C16H25NO4
Molecular Weight: 295.3740

Identification/Properties


Properties
BP:
449.023°C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
295.379g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
8
Exact Mass:
295.178g/mol
Monoisotopic Mass:
295.178g/mol
Topological Polar Surface Area:
67.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
308
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:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



Boc-D-Threoninol(Bzl) is a versatile compound widely used in chemical synthesis for the selective protection of the hydroxyl group in organic molecules. With its Boc (tert-butyloxycarbonyl) protecting group and benzyl (Bzl) ester functionalities, this compound plays a crucial role in the preparation of various complex molecules and peptidomimetics. By selectively masking the hydroxyl group in the threonine residue, Boc-D-Threoninol(Bzl) enables precise control over the reactivity of the molecule during multiple reaction steps, allowing chemists to synthesize diverse compounds with high specificity and efficiency. Its application extends to the synthesis of peptides, pharmaceuticals, and other bioactive molecules, making it a valuable tool in organic chemistry research and drug development.