656240-39-0

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

The compound is derived from 1,5-pentanediol by replacing one hydroxyl group with an acetate group.

Explanation

The compound has a specific spatial arrangement of atoms, with the 3S configuration indicating the orientation of the hydroxyl group on the chiral center.

Explanation

The structure of the compound consists of a five-carbon pentane chain, a benzene ring with a methyl group and methoxymethoxy substituents, and an acetate group attached to the 3S stereocenter.

Explanation

The compound is used in various industries, including the synthesis of pharmaceuticals, as a reagent in organic chemistry, and potentially in the formulation of cosmetics and personal care products.

Explanation

Due to potential hazards if mishandled, it is essential to follow safety guidelines and protocols when working with this chemical compound.

Monoacetate Derivative

1,5-Pentanediol

Stereoisomer

3S

Chemical Structure

Contains a pentane chain, a phenyl ring, and an acetate group

Applications

Pharmaceutical synthesis, organic chemical reactions, cosmetics, and personal care products

Safety Precautions

Handle with care and follow proper safety protocols

Upstream product

• 108-05-4 vinyl acetate 
• 656240-38-9 3-(3-methoxymethoxy-4-methyl-phenyl)-pentane-1,5-diol 
• 1027052-37-4 acetic acid 5-acetoxy-3-(3-methoxymethoxy-4-methyl-phenyl)-pentyl ester 
• 656240-50-5 4-iodo-2-methoxymethoxy-1-methyl-benzene 
• 656240-37-8 3-(3-methoxymethoxy-4-methyl-phenyl)-pent-4-en-1-ol 
• 656240-35-6 3-(3-methoxymethoxy-4-methyl-phenyl)-prop-2-yn-1-ol 

Downstream Products

• 656240-46-9 (3R,5S)-5-(2-Bromo-5-methoxymethoxy-4-methyl-phenyl)-7-(tert-butyl-diphenyl-silanyloxy)-2-methyl-heptane-2,3-diol 
• 656240-47-0 2-{(2R,4S)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-6-methoxymethoxy-7-methyl-chroman-2-yl}-propan-2-ol 
• 656240-45-8 (3R,5S)-7-(tert-Butyl-diphenyl-silanyloxy)-5-(3-methoxymethoxy-4-methyl-phenyl)-2-methyl-heptane-2,3-diol 
• 656240-42-5 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentanoic acid 
• 656240-44-7 tert-butyl-[3-(3-methoxymethoxy-4-methyl-phenyl)-6-methyl-hept-5-enyloxy]-diphenyl-silane 
• 656240-40-3 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentan-1-ol 
• 656240-41-4 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentanal 
• 656240-52-7 acetic acid 5-(tert-butyl-diphenyl-silanyloxy)-3-(3-methoxymethoxy-4-methyl-phenyl)-pentyl ester 

Relevant academic research and scientific papers

An Alternative Total Synthesis of (-)-Heliannuol E1

An efficient, enantiocontrolled total synthesis of (-)-heliannuol E has been accomplished using a palladium-catalyzed cyclization of the six-membered oxygen containing heterocycle as the key reaction step.