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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)-

Resorcinol-13C6

O[13c]1[13cH][13cH][13cH][13c]([13cH]1)O Request for Quotation
Chemical Name: Resorcinol-13C6
CAS Number: 953390-31-3
Product Number: AG005S4U(AGN-PC-0WAHYR)
Synonyms:
MDL No:
Molecular Formula: C6H6O2
Molecular Weight: 116.0666

Identification/Properties

Computed Properties
Molecular Weight:
116.066g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
116.057g/mol
Monoisotopic Mass:
116.057g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
64.9
Isotope Atom Count:
6
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Resorcinol-13C6, a unique isotope-labeled derivative of resorcinol, finds significant application in chemical synthesis as a versatile building block and tracer molecule. The incorporation of the stable 13C isotope in six positions of the resorcinol structure allows for precise tracking and elucidation of reaction mechanisms and pathways in complex organic transformations. This labeled compound serves as a powerful tool in isotope tracing studies, metabolic flux analysis, and structure-activity relationship investigations within the realm of organic chemistry and medicinal chemistry. Its application extends to the synthesis of labeled pharmaceuticals, agrochemicals, and specialty chemicals, enabling researchers to gain valuable insights into the behavior and transformation of molecules in biological systems and industrial processes.