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2,3-EPOXYDECANAL, with the molecular formula C10H18O2, is a chemical compound known for its distinctive fruity and floral scent. It is recognized for its potential as a biomarker for oxidative stress, antioxidant and anti-inflammatory properties, and its role in assessing environmental air quality and as a potential anti-cancer agent.

1048958-35-5

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1048958-35-5 Usage

Uses

Used in Perfumery and Fragrance Industry:
2,3-EPOXYDECANAL is used as a fragrance ingredient for its fruity and floral odor, contributing to the creation of various perfumes and scented products.
Used in Medical Research:
2,3-EPOXYDECANAL is used as a potential biomarker for oxidative stress in the body, helping in the study and detection of related health conditions.
Used in Environmental Science:
2,3-EPOXYDECANAL is used as an indicator for the presence of toxic aldehydes in the environment, serving as a tool to assess and monitor air quality.
Used in Cancer Research:
2,3-EPOXYDECANAL is used as a potential anti-cancer agent, being investigated for its ability to induce programmed cell death in certain cancer cells, which could lead to new therapeutic approaches.

Check Digit Verification of cas no

The CAS Registry Mumber 1048958-35-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,8,9,5 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1048958-35:
(9*1)+(8*0)+(7*4)+(6*8)+(5*9)+(4*5)+(3*8)+(2*3)+(1*5)=185
185 % 10 = 5
So 1048958-35-5 is a valid CAS Registry Number.

1048958-35-5Upstream product

1048958-35-5Relevant academic research and scientific papers

Organocatalytic asymmetric epoxidation and tandem epoxidation/Passerini reaction under eco-friendly reaction conditions

Deobald, Anna Maria,Corrêa, Arlene G.,Rivera, Daniel G.,Paix?o, Márcio Weber

, p. 7681 - 7684 (2012)

An eco-friendly synthesis of highly functionalized epoxides and their incorporation into an organocatalytic multicomponent approach are reported. For this, a modified class of diarylprolinol silyl ethers was designed to enable high catalytic activity in an environmentally benign solvent system. The one-pot procedure showed great efficiency in promoting stereoselective multicomponent transformations in a tandem, 'green' fashion. Because of its non-residual, efficient and selective character, this synthetic design shows promise for large-scale applications in both diversity and target-oriented syntheses. The Royal Society of Chemistry 2012.

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