19689-88-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Methoxy-6-nitro-benzaldehyde is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex organic molecules that can exhibit therapeutic effects.
Used in Organic Compounds Synthesis:
It serves as a key component in the synthesis of other organic compounds, where its chemical structure can be manipulated to create a variety of products with different applications.
Used in Dye and Pigment Production:
2-Methoxy-6-nitro-benzaldehyde is used as a precursor in the production of dyes and pigments, capitalizing on its color-producing properties to create a range of hues for various industries.
Safety Precautions:
Given its potentially hazardous nature, 2-Methoxy-6-nitro-benzaldehyde should be handled and stored with care, adhering to proper safety measures to mitigate risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 19689-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,8 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19689-88:
(7*1)+(6*9)+(5*6)+(4*8)+(3*9)+(2*8)+(1*8)=174
174 % 10 = 4
So 19689-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO4/c1-13-8-4-2-3-7(9(11)12)6(8)5-10/h2-5H,1H3
19689-88-4Relevant academic research and scientific papers
ALLOSTERIC ACTIVATORS OF THE ALPHA1A -ADRENERGIC RECEPTOR
-
, (2020/11/04)
The present invention relates to compounds that are activators of the Alpha1A-Adrenergic Receptor (α1A-AR) and methods of using such compounds: for treating neurological conditions, for cardio-protection, and for treating other condi
Effect of aldehyde and methoxy substituents on nucleophilic aromatic substitution by [18F]fluoride
Shen, Bin,L?ffler, Dirk,Zeller, Klaus-Peter,übele, Michael,Reischl, Gerald,Machulla, Hans-Jürgen
, p. 1461 - 1468 (2008/09/18)
For a series of benzaldehydes only with a leaving group or with both a leaving group and a single methoxy substituent 18F-fluorination via nucleophilic aromatic substitution (SNAr) was studied in DMF and Me2SO. In general, the radiochemical yields were clearly higher in DMF than in Me2SO. In the fluorodehalogenation reaction (leaving group: halogen = Br, Cl), extremely low radiochemical yields were observed in Me2SO (2SO (within 3 min reaction time, 90% of the precursor was consumed; radiochemical yield = 1.0 ± 0.5%); however, in DMF oxidation was always kept at a low level during the entire reaction (13C-NMR ppm values of the aromatic carbon atom bearing the leaving group.
