27247-34-3 Usage
Description
Potassium 5-(Methoxycarbonyl)nicotinate, also known as 5-(Methoxycarbonyl)nicotinic Acid Potassium Salt, is an organic compound that serves as an intermediate in the synthesis of various chemical compounds. It is characterized by its ability to form salts and esters, which makes it a versatile compound in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
Potassium 5-(Methoxycarbonyl)nicotinate is used as an intermediate in the synthesis of Nornicotine (N757000) analogs. These analogs are employed as haptens for immunoassays, which are essential tools in the detection and measurement of specific substances, particularly in the fields of drug testing, medical diagnostics, and environmental monitoring.
Used in Chemical Synthesis:
In the chemical industry, Potassium 5-(Methoxycarbonyl)nicotinate is utilized as a key intermediate in the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its ability to form salts and esters makes it a valuable building block in the development of new molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 27247-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,4 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27247-34:
(7*2)+(6*7)+(5*2)+(4*4)+(3*7)+(2*3)+(1*4)=113
113 % 10 = 3
So 27247-34-3 is a valid CAS Registry Number.
27247-34-3Relevant articles and documents
A predictive model for additions to: N -alkyl pyridiniums
Knight, Brian J.,Tolchin, Zachary A.,Smith, Joel M.
supporting information, p. 2693 - 2696 (2021/03/18)
Disclosed in this communication is a thorough study on the dearomative addition of organomagnesium nucleophiles to N-alkyl pyridinium electrophiles. The regiochemical outcomes have observable and predictable trends associated with the substituent patterns on the pyridinium electrophile. Often, the substituent effects can be either additive, giving high selectivities, or ablative, giving competing outcomes. Additionally, the nature of the organometallic nucleophilic component was also investigated for its role in the regioselective outcome. The effects of either reactive component are important to both the overall reactivity and site of nucleophilic addition. The utility of these observed trends is demonstrated in a concise, dearomative synthesis of a tricyclic compound shown to have insecticidal activity. This journal is
