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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)-

2,4-Dodecadien-1-ol, (2E,4E)-

CCCCCCC/C=C/C=C/CO Request for Quotation
Chemical Name: 2,4-Dodecadien-1-ol, (2E,4E)-
CAS Number: 18485-38-6
Product Number: AG003EO8(AGN-PC-0O5BXJ)
Synonyms:
MDL No:
Molecular Formula: C12H22O
Molecular Weight: 182.3025

Identification/Properties

Properties
MP:
27 °C
Form:
Liquid
Computed Properties
Molecular Weight:
182.307g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
8
Exact Mass:
182.167g/mol
Monoisotopic Mass:
182.167g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
136
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
2
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Dodeca-2,4-dien-1-ol, also known as dodeca-2,4-dienol, is a valuable compound used in chemical synthesis for its versatile applications. This unsaturated alcohol serves as a crucial building block in the organic chemistry realm, particularly in the production of various compounds through different chemical reactions. Its unique structure and reactivity make it highly desirable for synthesizing intricate molecules with specific functionalities and properties. In organic synthesis, dodeca-2,4-dien-1-ol can participate in reactions such as oxidation, reduction, esterification, and many more, enabling the creation of a wide array of products ranging from fragrances to pharmaceuticals. Its use as a precursor in the synthesis of fine chemicals and specialty materials underscores its significance in modern chemical research and development.