CAS 5422-01-5

1-(1,3-benzodioxol-5-yl)pentan-1-ol

Description:

1-(1,3-benzodioxol-5-yl)pentan-1-ol, with the CAS number 5422-01-5, is an organic compound characterized by its structure, which features a pentanol chain attached to a benzodioxole moiety. This compound typically exhibits properties associated with both alcohols and aromatic compounds. It is likely to be a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of the hydroxyl (-OH) group imparts hydrophilic characteristics, allowing it to engage in hydrogen bonding, which can influence its solubility in polar solvents. The benzodioxole ring contributes to its aromaticity, potentially affecting its reactivity and stability. This compound may be of interest in various fields, including pharmaceuticals and organic synthesis, due to its potential biological activity and utility as a building block in chemical reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₂H₁₆O₃

InChI: InChI=1/C12H16O3/c1-2-3-4-10(13)9-5-6-11-12(7-9)15-8-14-11/h5-7,10,13H,2-4,8H2,1H3

SMILES: CCCCC(c1ccc2c(c1)OCO2)O

α-Butylpiperonyl Alcohol

Controlled Product

CAS: 5422-01-5

Applications Intermediate in the preparation of insecticides, fungicides, and other pesticides.
References Wilkinson, C., et al.: J. Agric. Food Chem., 14, 73 (1966), Zhong, W., et al.: J. Chem. Res., 6, 370 (2009),

Formula: C₁₂H₁₆O₃

Color and Shape: Neat

Molecular weight: 208.25

Ref: TR-B693695

a-Butylpiperonyl alcohol

Controlled Product

CAS: 5422-01-5

a-Butylpiperonyl alcohol is a chiral molecule that is used in the synthesis of esters. It can be produced by microbial fermentation and low-temperature chemical reactions. This compound has been shown to inhibit the growth of Gram-positive bacteria, such as Staphylococcus aureus and Streptococcus pneumoniae. The biosynthetic pathway for a-butylpiperonyl alcohol is not yet well understood, but it has been hypothesized that this compound is synthesized from an intermediate, acetic acid. The enzyme responsible for this conversion is unknown, but it may be catalysed by an acylase or acetate kinase. A study on the genome sequence of Coelicolor revealed that this organism produces a-butylpiperonyl alcohol from the intermediate 3-hydroxypropanoic acid.

Formula: C₁₂H₁₆O₃

Purity: Min. 95%

Molecular weight: 208.25 g/mol

Ref: 3D-FB19588