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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'-Biazetidin]-3-ol oxalate

OC(=O)C(=O)O.OC1CN(C1)C1CNC1 Request for Quotation
Chemical Name: [1,3'-Biazetidin]-3-ol oxalate
CAS Number: 1523606-25-8
Product Number: AG00HY0F(AGN-PC-0WCJNK)
Synonyms:
MDL No:
Molecular Formula: C8H14N2O5
Molecular Weight: 218.2072

Identification/Properties

Computed Properties
Molecular Weight:
218.209g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
2
Exact Mass:
218.09g/mol
Monoisotopic Mass:
218.09g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
179
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


[1,3'-Biazetidin]-3-ol oxalate, a novel and versatile organic compound, serves as a valuable reagent in chemical synthesis, particularly in the development of pharmaceuticals and specialty chemicals. Its unique molecular structure confers a range of reactivity and selectivity that makes it a promising candidate for various synthetic transformations. In organic synthesis, [1,3'-Biazetidin]-3-ol oxalate can act as a key building block for creating complex molecular architectures with specific functionalities. Its utility extends to the formation of heterocyclic compounds and the construction of biologically active molecules. Researchers and chemists leverage the reactivity of [1,3'-Biazetidin]-3-ol oxalate to access new chemical entities and optimize synthetic routes for the production of target compounds with enhanced properties. By incorporating this compound into synthetic strategies, the potential for discovering novel drug candidates or advanced materials is significantly heightened.