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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)-

4-Hexen-1-ol, (4Z)-

C/C=CCCCO Request for Quotation
Chemical Name: 4-Hexen-1-ol, (4Z)-
CAS Number: 928-91-6
Product Number: AG003OZA(AGN-PC-0ONGX4)
Synonyms:
MDL No:
Molecular Formula: C6H12O
Molecular Weight: 100.15888

Identification/Properties

Properties
Storage:
Room Temperature;Inert atmosphere;
Computed Properties
Molecular Weight:
100.161g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
3
Exact Mass:
100.089g/mol
Monoisotopic Mass:
100.089g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
48.1
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H227-H319
Precautionary Statements:
P210-P264-P280-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4Z)-4-Hexen-1-ol, also known as 4-Hexen-1-ol with a trans configuration, is a versatile compound widely used in chemical synthesis applications. Due to its unique structure and functional groups, (4Z)-4-Hexen-1-ol is employed as a valuable building block in the preparation of various organic compounds. Its primary application lies in the field of organic chemistry, where it serves as a key intermediate in the synthesis of fragrances, flavors, and pharmaceuticals.One of the significant uses of (4Z)-4-Hexen-1-ol is as a starting material for the synthesis of esters through esterification reactions. By reacting (4Z)-4-Hexen-1-ol with carboxylic acids in the presence of suitable catalysts, a wide range of ester compounds can be produced. These esters are essential in the fragrance and flavor industries, imparting pleasant aromas and tastes to various products.Additionally, (4Z)-4-Hexen-1-ol can participate in Diels-Alder reactions to form cyclic compounds with high regio- and stereoselectivity. This reaction is valuable in the production of complex organic molecules with multiple functionalities, making (4Z)-4-Hexen-1-ol a valuable tool in the synthesis of natural products and bioactive compounds.In summary, (4Z)-4-Hexen-1-ol plays a crucial role in chemical synthesis, enabling the creation of diverse compounds with applications in fragrance, flavor, pharmaceuticals, and other industries. Its versatility and reactivity make it a valuable asset for organic chemists seeking to design novel molecules and enhance the functionality of existing compounds.