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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)-

5-Hepten-3-ynoic acid,2,2-dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-, (5E)-

CN(Cc1cccc2c1cccc2)C/C=C/C#CC(C(=O)O)(C)C Request for Quotation
Chemical Name: 5-Hepten-3-ynoic acid,2,2-dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-, (5E)-
CAS Number: 99473-14-0
Product Number: AG0065GO(AGN-PC-0W9FZQ)
Synonyms:
MDL No:
Molecular Formula: C21H23NO2
Molecular Weight: 321.4128

Identification/Properties

Properties
MP:
118 - 120°C
Storage:
2-8℃;Keep in dry area;
Form:
Solid
Computed Properties
Molecular Weight:
321.42g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
6
Exact Mass:
321.173g/mol
Monoisotopic Mass:
321.173g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
522
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


(5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid is a valuable compound widely used in chemical synthesis due to its unique properties and versatile applications. This compound serves as a key building block in the synthesis of various bioactive molecules, pharmaceuticals, and organic compounds.In chemical synthesis, (5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid acts as a precursor for the preparation of novel compounds with potential biological activities. Its functional groups and stereochemistry make it an ideal starting material for the creation of complex molecular structures through organic transformations. By utilizing this compound in synthesis, chemists can access a diverse array of chemical derivatives with tailored properties and functionalities.Additionally, (5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid plays a crucial role in the development of new drugs, agrochemicals, and materials with specific applications. Its incorporation into molecular frameworks can lead to the discovery of compounds with enhanced biological or physical properties, making it a valuable tool in the field of chemical research and innovation.Overall, the application of (5E)-2,2-Dimethyl-7-[methyl(1-naphthalenylmethyl)amino]-5-hepten-3-ynoic acid in chemical synthesis opens up exciting possibilities for the design and creation of novel compounds with diverse functions and potential societal impact.