10273-40-2 Usage
Uses
Used in Pharmaceutical Synthesis:
2,7-Naphthyridine-4-carbaldehyde is used as a building block in the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the preparation of complex molecules with potential therapeutic properties.
Used in Agrochemical Production:
In the agrochemical industry, 2,7-naphthyridine-4-carbaldehyde serves as a key intermediate for the development of new compounds with pesticidal or herbicidal properties, contributing to more effective and targeted crop protection solutions.
Used in Fine Chemicals Synthesis:
2,7-Naphthyridine-4-carbaldehyde is utilized as a versatile intermediate in the synthesis of a wide range of fine chemicals, including specialty dyes, fragrances, and other high-value organic compounds.
Used in Fluorescent Probes and Dyes Development:
Leveraging its fluorescent properties, 2,7-naphthyridine-4-carbaldehyde is used as a starting material in the development of fluorescent probes and dyes for bioimaging applications. These probes and dyes can be employed in various research and diagnostic fields to visualize and study biological processes at the molecular level.
Check Digit Verification of cas no
The CAS Registry Mumber 10273-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10273-40:
(7*1)+(6*0)+(5*2)+(4*7)+(3*3)+(2*4)+(1*0)=62
62 % 10 = 2
So 10273-40-2 is a valid CAS Registry Number.
10273-40-2Relevant academic research and scientific papers
Vilsmeier-Haack reaction of tertiary alcohols: Formation of functionalised pyridines and naphthyridines
Thomas,Asokan
, p. 2583 - 2587 (2007/10/03)
Vilsmeier-Haack reaction of 2-arylpropan-2-ols proceeds with multiple iminoalkylations leading to the formation of conjugated iminium salts which on ammonium acetate-induced cyclisation afford 4-arylnicotinaldehydes in good yields. Tertiary alcohols derived from aliphatic or alicyclic ketones by the addition of methyl Grignard are converted into substituted pyridines and naphthyridines by the action of Vilsmeier's reagent in N,N-dimethylformamide followed by nucleophile-assisted cyclisation in the presence of ammonium acetate.
