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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)-

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

OC[C@H]([C@H](OCc1ccccc1)C)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: Carbamic acid, [(1R,2R)-1-(hydroxymethyl)-2-(phenylmethoxy)propyl]-,1,1-dimethylethyl ester
CAS Number: 133565-43-2
Product Number: AG003UIQ(AGN-PC-0PK0NT)
Synonyms:
MDL No:
Molecular Formula: C16H25NO4
Molecular Weight: 295.3740

Identification/Properties

Properties
BP:
449.023°C at 760 mmHg
Storage:
Keep in dry area;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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Boc-Thr(Bzl)-ol, also known as N-Boc-L-threoninol benzyl ester, is a versatile compound commonly used in chemical synthesis. This protected amino alcohol serves as a crucial building block in organic chemistry, particularly in peptide synthesis and drug development.Its Boc (tert-butoxycarbonyl) protecting group shields the amino group of threonine, preventing unwanted reactions during synthesis. The benzyl ester on the alcohol group also offers protection and can be selectively removed under mild conditions when needed. This selective deprotection functionality makes Boc-Thr(Bzl)-ol highly valuable in peptide coupling reactions, where precise and controlled manipulation of functional groups is essential.Furthermore, Boc-Thr(Bzl)-ol can be utilized in the preparation of various amino acid derivatives, pharmaceutical intermediates, and complex natural product syntheses. Its compatibility with a wide range of reagents and reaction conditions makes it a valuable tool in the toolbox of synthetic chemists.