40500-10-5 Usage
Uses
Due to the limited information available on 3-(Tetrahydro-2H-pyran-4-yl)propanoic acid, its applications are not well-defined. However, based on its chemical structure, it can be hypothesized that it may have potential uses in various industries, such as:
Used in Pharmaceutical Industry:
3-(Tetrahydro-2H-pyran-4-yl)propanoic acid could be used as an intermediate compound for the synthesis of pharmaceutical drugs, given its heterocyclic nature and carboxylic acid group. 3-(TETRAHYDRO-2H-PYRAN-4-YL)PROPANOIC ACID's unique chemical behavior may allow it to form new drug molecules with potential therapeutic applications.
Used in Chemical Research:
3-(Tetrahydro-2H-pyran-4-yl)propanoic acid may serve as a subject of study in chemical research, particularly in the field of organic chemistry. Its structure and properties could provide insights into the behavior of heterocyclic compounds and their potential applications in various chemical processes.
Used in Material Science:
3-(TETRAHYDRO-2H-PYRAN-4-YL)PROPANOIC ACID's unique structure may also make it a candidate for use in material science, where it could be explored for its potential to contribute to the development of new materials with specific properties, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 40500-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40500-10:
(7*4)+(6*0)+(5*5)+(4*0)+(3*0)+(2*1)+(1*0)=55
55 % 10 = 5
So 40500-10-5 is a valid CAS Registry Number.
40500-10-5Relevant academic research and scientific papers
METHOD OF MAKING AZAINDAZOLE DERIVATIVES
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, (2012/05/04)
Disclosed are methods, reagents, and intermediates useful for making azaindazole derivatives, which may be used to modulate Glucokinase. The disclosed methods and materials are generally useful for making halo-esters and sulfonyl-substituted compounds.
One-pot conversion of alkyl aldehydes into substituted propanoic acids via Knoevenagel condensation with Meldrum's acid
Mudhar, Harminder,Witty, Andrew
experimental part, p. 4972 - 4974 (2011/01/12)
Reaction of a range of alkyl aldehydes and Meldrum's acid in triethylammonium formate (TEAF) at 100 °C generates substituted propanoic acids in a single step.
