35847-32-6 Usage
Structure
A five-membered heterocyclic compound containing three nitrogen atoms with an ester functional group attached to the 1-position of the triazole ring.
Functional Groups
Triazole, carboxylic acid, and ethyl ester.
Solubility
More soluble in organic solvents due to the presence of the ethyl ester group.
Organic synthesis
Used as an intermediate in the synthesis of various organic compounds.
Medicinal chemistry
Studied for potential applications in drug discovery and development.
Anti-fungal agents
Investigated for its potential use in the development of antifungal drugs.
Anti-tumor agents
Explored for its potential role in the development of anti-cancer drugs.
Building block
Utilized as a building block in the synthesis of pharmaceuticals and agrochemicals.
Significance
Plays a crucial role in the development and production of various chemical and pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 35847-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,4 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35847-32:
(7*3)+(6*5)+(5*8)+(4*4)+(3*7)+(2*3)+(1*2)=136
136 % 10 = 6
So 35847-32-6 is a valid CAS Registry Number.
35847-32-6Relevant academic research and scientific papers
1,3-DIPOLAR CYCLOADDITIONS TO 2,3-DIMETHOXYCARBONYL-7-OXABICYCLO-2,5-HEPTADIENE, 1,4-EPOXY-1,4-DIHYDRONAPHTHALENE, AND exo-endo-1,6-DIMETHOXYCARBONYL-11,12-DIOXATETRACYCLO2,5,17,10>-3,8-DODECADIENE
Fisera, L'ubor,Pavlovic, Dusan
, p. 1990 - 2000 (2007/10/02)
The paper deals with site-selectivity of l,3-dipolar cycloadditions of ethyl azidoformate, azidoacetate, and diazo acetate to 2,3-dimethoxycarbonyl-7-oxabicyclo-2,5-heptadiene.The exo-endo stereoselectivity has been studied of the reactions of 1,4-
