10024-70-1 Usage
Description
3-methoxybutyric acid, also known as MBHA, is a short-chain fatty acid characterized by a butyric acid group with a methoxy group attached to the third carbon. It is naturally found in certain foods and is produced as a metabolite in the human body. MBHA has garnered interest for its potential therapeutic effects, particularly in the treatment of metabolic disorders, due to its role in regulating energy metabolism and insulin sensitivity. Additionally, it has been studied as a biomarker for metabolic diseases and as a precursor for the synthesis of pharmaceutical compounds, showcasing its promise in medicine and drug development.
Uses
Used in Pharmaceutical Development:
3-methoxybutyric acid is used as a precursor for the synthesis of pharmaceutical compounds, leveraging its chemical properties to create new medications.
Used in Metabolic Disorder Treatment:
3-methoxybutyric acid is used as a therapeutic agent for metabolic disorders, capitalizing on its role in regulating energy metabolism and improving insulin sensitivity.
Used in Biomarker Research:
3-methoxybutyric acid is used as a potential biomarker for metabolic diseases, given its presence in the human body and its association with metabolic processes.
Used in Nutritional Supplements:
Although not explicitly mentioned in the provided materials, MBHA's natural occurrence in certain foods and its potential health benefits could position it as an ingredient in nutritional supplements aimed at supporting metabolic health.
Check Digit Verification of cas no
The CAS Registry Mumber 10024-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,2 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10024-70:
(7*1)+(6*0)+(5*0)+(4*2)+(3*4)+(2*7)+(1*0)=41
41 % 10 = 1
So 10024-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O3/c1-4(8-2)3-5(6)7/h4H,3H2,1-2H3,(H,6,7)
10024-70-1Relevant articles and documents
Some 4 oxa farnesane insect juvenile hormone mimics
Patwardhan,Gupta,Dev
, p. 697 - 702 (1976)
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Iridium-catalyzed asymmetric hydrogenation of vinyl ethers
Zhu, Ye,Burgess, Kevin
supporting information; experimental part, p. 979 - 983 (2009/05/30)
A carbene-oxazoline catalyst 1 proved to be an effective catalyst for reduction of an enol ether that the literature suggested could not be hydrogenated effectively by P,N-Ir catalysts. Thus, a series of ester and alcohol substrates were hydrogenated using catalyst 1. Good to excellent enantioselectivities and high conversions were obtained.
Halogenated Epoxides. 61. Reactions of Selected Chlorooxiranes with Sodium Methoxide: About the Question of Acetylenic and Allenic Epoxides as Intermediates
Griesbaum, Karl,Lie, Giu Oan,Keul, Helmut
, p. 679 - 682 (2007/10/02)
Reactions of sodium methoxide with five chlorooxiranes (1, 3, 11, 18, and 19) and with the corresponding isomeric chlorocarbonyl compounds have been examined.In two cases the chlorooxirane and the corresponding chlorocarbonyl compound afforded the same products, however, in different yields.In the other cases the chlorooxiranes and the corresponding chlorocarbonyl compounds gave different products.It is concluded that chlorocarbonyl compounds are not formed to a large extent as intermediates.In the reactions of two chlorooxiranes (18 and 19) with sodium methoxide, acetylenic and allenic epoxides may be invoked as transient intermediates.
