13022-85-0 Usage
Description
2-KETOHEXANOIC ACID SODIUM SALT is an organic compound that acts as a precursor to the synthesis of various pharmaceuticals and chemicals. It is known for its ability to induce insulin secretion and increase the fluorescence of NADPH in perfused isolated mouse pancreatic islets.
Uses
Used in Pharmaceutical Industry:
2-KETOHEXANOIC ACID SODIUM SALT is used as a precursor in the synthesis of various pharmaceuticals and chemicals for its ability to induce insulin secretion and increase the fluorescence of NADPH in perfused isolated mouse pancreatic islets.
Used in Diabetes Research:
2-KETOHEXANOIC ACID SODIUM SALT is used as a research compound for studying the mechanisms of insulin secretion and the role of NADPH in pancreatic islets, which can contribute to the development of new treatments for diabetes.
Check Digit Verification of cas no
The CAS Registry Mumber 13022-85-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,2 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13022-85:
(7*1)+(6*3)+(5*0)+(4*2)+(3*2)+(2*8)+(1*5)=60
60 % 10 = 0
So 13022-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3.Na/c1-2-3-4-5(7)6(8)9;/h2-4H2,1H3,(H,8,9);
13022-85-0Relevant articles and documents
Dioxolanones as Synthetic Intermediates. Part 1. Synthesis of α-Keto Acids, α-Keto Aldehydes, and α-Ketols
Ramage, Robert,Griffiths, Gareth J.,Shutt, Fiona E.,Sweeney, John N. A.
, p. 1531 - 1537 (2007/10/02)
2,2-Pentamethylene-1,3-dioxolan-4-one (10) has been elaborated to provide 5'-ylidene derivatives using a Wittig approach.This apparently novel class of compounds is subject to nucleophilic attack at the 4-position because of strain inherent in the 5-membered ring.Thus alkaline hydrolysis leads to the formation of α-keto acids; hydride reduction of dioxolanones incorporating conjugated aryl substituents using di-isobutylaluminium hydride leads to α-keto-aldehydes; the reaction of dioxolanone (15) with methylmagnesium iodide gave the α-ketol (40).
