2734-70-5 Usage
Description
2,6-DIMETHOXYANILINE is an organic compound with the chemical formula C8H11NO2. It is an off-white solid and is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Chemical Research:
2,6-DIMETHOXYANILINE is used as a research compound for studying the degradation process of 2,6-dimethylaniline through the Fenton process. This helps in understanding the reactions involved in the oxidation of 2,6-dimethylaniline under various reaction conditions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-DIMETHOXYANILINE is used as a starting material for the synthesis of various drugs, such as local anesthetics like lidocaine. It is used as a precursor for the production of these drugs due to its reactivity and compatibility with other chemical compounds.
Used in Analytical Chemistry:
2,6-DIMETHOXYANILINE is used as a reference compound in the development of gas chromatographic-mass spectrometric assays. It helps in the detection of hemoglobin adducts covalently bound to rat hemoglobin after administration of either 2,6-dimethylaniline or lidocaine, which is crucial for understanding the metabolic pathways and potential toxic effects of these compounds.
Used in Environmental Applications:
2,6-DIMETHOXYANILINE can be used in environmental applications for the study of pollutant degradation and removal processes. Its reactivity and chemical properties make it a suitable candidate for investigating the effectiveness of various treatment methods in reducing the environmental impact of pollutants.
Check Digit Verification of cas no
The CAS Registry Mumber 2734-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2734-70:
(6*2)+(5*7)+(4*3)+(3*4)+(2*7)+(1*0)=85
85 % 10 = 5
So 2734-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO2/c1-10-6-4-3-5-7(11-2)8(6)9/h3-5H,9H2,1-2H3
2734-70-5Relevant articles and documents
Nickel(ii)-catalyzed asymmetric thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles
Yang, Wei,Lin, Xiaobin,Zhang, Yongyan,Cao, Weidi,Liu, Xiaohua,Feng, Xiaoming
, p. 10002 - 10005 (2020/09/15)
A nickel(ii) catalyzed enantioselective thio-Claisen rearrangement of α-diazo pyrazoleamides with thioindoles was realized with modified chiral N,N′-dioxide ligands, affording a variety of C3-substituted indole derivatives in high yields (up to 95%) with excellent enantioselectivities (up to 96% ee) under mild reaction conditions. A possible transition state model was proposed based on previous reports and the X-ray crystal structure of the catalyst.
Kolbe-Schmitt type reaction under ambient conditions mediated by an organic base
Sadamitsu, Yuta,Okumura, Akira,Saito, Kodai,Yamada, Tohru
, p. 9837 - 9840 (2019/08/20)
The combined use of an organic base for resorcinols realized a Kolbe-Schmitt type reaction under ambient conditions. When resorcinols (3-hydroxyphenol derivatives) were treated with DBU under a carbon dioxide atmosphere, nucleophilic addition to carbon dioxide proceeded to afford the corresponding salicylic acid derivatives in high yields.
Cu(II)-Mediated N-H and N-Alkyl Aryl Amination and Olefin Aziridination
Munnuri, Sailu,Anugu, Raghunath Reddy,Falck, John R.
supporting information, p. 1926 - 1929 (2019/03/11)
Cu(II)-mediated direct NH2 and NH alkyl aryl aminations and olefin aziridinations are described. These room-temperature, one-pot, environmentally friendly procedures replace costly Rh2 catalysts and, in some instances, display important differences with comparable Rh2- and Fe-supported reactions.
