99414-71-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2,3-Dibromohexanal is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Organic Compound Synthesis:
This chemical serves as an intermediate in the synthesis of other organic compounds, playing a crucial role in the creation of a wide range of chemical products.
Used in Laboratory Experiments:
2,3-Dibromohexanal is employed as a chemical reagent in various laboratory settings, facilitating research and experimentation across different scientific disciplines.
Used in Agricultural and Industrial Settings:
With its demonstrated antimicrobial properties, 2,3-dibromohexanal has potential applications in agriculture and industry, where it could be used for its preservative qualities.
Used as a Preservative in Food and Cosmetic Products:
2,3-Dibromohexanal is being studied for its potential use as a preservative in food and cosmetic products, capitalizing on its antimicrobial properties to extend shelf life and maintain product integrity.
Check Digit Verification of cas no
The CAS Registry Mumber 99414-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,1 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99414-71:
(7*9)+(6*9)+(5*4)+(4*1)+(3*4)+(2*7)+(1*1)=168
168 % 10 = 8
So 99414-71-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10Br2O/c1-2-3-5(7)6(8)4-9/h4-6H,2-3H2,1H3
99414-71-8Relevant academic research and scientific papers
Rozema, Michael J.,Eisenberg, Christina,Luetjens, Henning,Ostwald, Roswitha,Belyk, Kevin,Knochel, Paul
, p. 3115 - 3118 (1993)
Catalytic amounts of Cu(I) salts considerably facilitate the iodine-zinc exchange reaction leading to polyfunctional dialkylzincs.The catalytic asymmetric addition of these zinc reagents to a wide range of α,β-unsaturated aldehydes provides polyfunctional allylic alcohols with a high enantioselectivity.