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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)-

1,3-Butanediol, 2-amino-, (R*,R*)-

OC[C@H]([C@H](O)C)N Request for Quotation
Chemical Name: 1,3-Butanediol, 2-amino-, (R*,R*)-
CAS Number: 3228-51-1
Product Number: AG003542(AGN-PC-0O8WKX)
Synonyms:
MDL No:
Molecular Formula: C4H11NO2
Molecular Weight: 105.1356

Identification/Properties

Properties
MP:
49-54 °C(lit.);
BP:
257.8°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
105.137g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
105.079g/mol
Monoisotopic Mass:
105.079g/mol
Topological Polar Surface Area:
66.5A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
49
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#:
N/A
Hazard Statements:
H315-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


L-Threoninol, also known as (2S,3R)-2-amino-3-hydroxybutanol, is a versatile compound widely used in chemical synthesis for various applications in the field of organic chemistry. Its hydroxyl and amino groups make it a valuable building block for the synthesis of complex molecules with biological activity. In organic chemistry, L-Threoninol serves as a chiral starting material for the preparation of enantiopure compounds and pharmaceutical intermediates. Its stereochemical properties play a crucial role in the development of new drugs, ligands, and other fine chemicals. With its unique structure, L-Threoninol offers a strategic advantage in designing and synthesizing molecules with specific chirality, enhancing their potential for use in advanced materials, drug discovery, and various chemical processes.