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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-oxazolidine-4-carboxylic acid;hydrochloride

OC(=O)C1COCN1.Cl Request for Quotation
Chemical Name: 1,3-oxazolidine-4-carboxylic acid;hydrochloride
CAS Number: 162285-30-5
Product Number: AG001SYI(AGN-PC-07CF50)
Synonyms:
MDL No:
Molecular Formula: C4H8ClNO3
Molecular Weight: 153.5642

Identification/Properties

Computed Properties
Molecular Weight:
153.562g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
153.019g/mol
Monoisotopic Mass:
153.019g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
104
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
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


(S)-Oxazolidine-4-carboxylic acid hydrochloride is a versatile chemical compound that finds significant application in chemical synthesis. This compound serves as a key building block in the creation of various compounds and materials due to its unique structural properties. In organic synthesis, (S)-Oxazolidine-4-carboxylic acid hydrochloride is commonly employed as a chiral auxiliary, aiding in the asymmetric synthesis of important molecules by controlling the stereochemistry of reactions. Additionally, this compound can act as a precursor in the preparation of complex molecules such as pharmaceutical intermediates and agrochemicals. Its ability to impart chirality to reactions makes it a valuable tool for chemists working in the field of organic chemistry. By utilizing (S)-Oxazolidine-4-carboxylic acid hydrochloride in chemical synthesis, researchers can access a diverse array of chiral compounds with high selectivity and efficiency.