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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-Hexen-1-ol, (2Z)-

CCC/C=CCO Request for Quotation
Chemical Name: 2-Hexen-1-ol, (2Z)-
CAS Number: 928-94-9
Product Number: AG00IHC7(AGN-PC-0ONGYR)
Synonyms:
MDL No:
Molecular Formula: C6H12O
Molecular Weight: 100.15888

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1987
Hazard Statements:
H226
Precautionary Statements:
P501-P240-P210-P233-P243-P241-P242-P280-P370+P378-P303+P361+P353-P403+P235
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cis-2-hexen-1-ol, also known as (Z)-2-hexen-1-ol, is a versatile compound used in various chemical synthesis processes. This compound is commonly employed as a starting material or intermediate in the production of fragrances, flavors, and pharmaceuticals. Its unique chemical structure, characterized by a cis double bond and a hydroxyl group, allows for a wide range of reactions and functional group transformations.In chemical synthesis, cis-2-hexen-1-ol can serve as a precursor for the synthesis of various esters through esterification reactions. By reacting with carboxylic acids in the presence of an acid catalyst, cis-2-hexen-1-ol can be converted into esters with different functional groups, imparting characteristic scents and flavors. Additionally, this compound can undergo oxidation reactions to produce aldehydes or carboxylic acids, further expanding its synthetic utility.Furthermore, cis-2-hexen-1-ol can participate in cross-coupling reactions to form carbon-carbon bonds with other organic molecules. This property enables the synthesis of more complex compounds and can be utilized in the construction of natural products and bioactive molecules. Overall, the application of cis-2-hexen-1-ol in chemical synthesis showcases its significance as a valuable building block for the creation of various compounds with diverse functionalities.