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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)-

3-Azetidinecarboxylic acid, 1-[(4-methylphenyl)sulfonyl]-

OC(=O)C1CN(C1)S(=O)(=O)c1ccc(cc1)C Request for Quotation
Chemical Name: 3-Azetidinecarboxylic acid, 1-[(4-methylphenyl)sulfonyl]-
CAS Number: 92993-58-3
Product Number: AG00IHFA(AGN-PC-02RA6Y)
Synonyms:
MDL No:
Molecular Formula: C11H13NO4S
Molecular Weight: 255.2902

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
255.288g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
255.057g/mol
Monoisotopic Mass:
255.057g/mol
Topological Polar Surface Area:
83.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
386
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
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


1-Tosylazetidine-3-carboxylic acid is a versatile building block commonly used in chemical synthesis. It is widely employed in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique chemical reactivity and structural properties.This compound serves as a valuable intermediate in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development. In particular, 1-Tosylazetidine-3-carboxylic acid can undergo various chemical transformations, such as nucleophilic substitution, ring-closure reactions, and functional group manipulations, to introduce specific molecular functionalities required for target molecule synthesis.Furthermore, the azetidine ring present in this compound offers structural diversity and rigidity, making it a key component in designing bioactive molecules with improved pharmacological properties. By incorporating 1-Tosylazetidine-3-carboxylic acid into synthetic routes, chemists can efficiently access complex molecular scaffolds and optimize the biological activity of the final products.Overall, the strategic utilization of 1-Tosylazetidine-3-carboxylic acid in chemical synthesis enables researchers to expedite the development of innovative compounds with potential applications in the fields of medicine, agriculture, and materials science.