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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)-

3,6,9,12,15,18,21-Heptaoxatricosan-1-ol, 23-azido-

OCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-] Request for Quotation
Chemical Name: 3,6,9,12,15,18,21-Heptaoxatricosan-1-ol, 23-azido-
CAS Number: 352439-36-2
Product Number: AG003TEQ(AGN-PC-0NDJ4K)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
395.453g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
10
Rotatable Bond Count:
23
Exact Mass:
395.227g/mol
Monoisotopic Mass:
395.227g/mol
Topological Polar Surface Area:
99.2A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
333
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 23-Azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol serves as a versatile building block in chemical synthesis, particularly in the field of organic chemistry. Due to its unique structure and functional groups, it is widely employed as a precursor in the synthesis of various complex organic molecules and polymers. The azido group (-N3) present in the compound is a key feature that enables it to participate in important reactions such as azide-alkyne cycloaddition (Click chemistry), allowing for the efficient and selective formation of new carbon–nitrogen bonds. Additionally, the hydroxyl group (-OH) offers further possibilities for derivatization through various chemical transformations, expanding the compound's utility in the development of novel materials and bioactive compounds. The strategic incorporation of 23-Azido-3,6,9,12,15,18,21-heptaoxatricosan-1-ol into synthetic routes enables researchers to access a diverse range of target molecules with potential applications in pharmaceuticals, materials science, and other chemical industries.