115210-53-2 Usage
Description
2,3-dihydro-1-Methyl-6-nitro-1H-Indole is a chemical compound with the molecular formula C9H9N3O2. It is a derivative of indole that contains a methyl group at the 1-position and a nitro group at the 6-position. 2,3-dihydro-1-Methyl-6-nitro-1H-Indole is a yellow to brown solid that is soluble in organic solvents.
Uses
Used in Pharmaceutical Industry:
2,3-dihydro-1-Methyl-6-nitro-1H-Indole is used as a chemical intermediate for the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows it to be a key component in the development of new drugs and medications.
Used in Agricultural Chemicals:
2,3-dihydro-1-Methyl-6-nitro-1H-Indole may have potential applications in the field of agricultural chemicals, where it could be used as a starting material for the synthesis of pesticides, herbicides, or other agrochemicals.
Used in Materials Science:
2,3-dihydro-1-Methyl-6-nitro-1H-Indole may also find use in materials science, where it could be employed in the development of new materials with specific properties, such as improved stability or reactivity. Its potential applications in this field are still being explored.
Check Digit Verification of cas no
The CAS Registry Mumber 115210-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115210-53:
(8*1)+(7*1)+(6*5)+(5*2)+(4*1)+(3*0)+(2*5)+(1*3)=72
72 % 10 = 2
So 115210-53-2 is a valid CAS Registry Number.
115210-53-2Relevant articles and documents
Ir-Catalyzed Reversible Acceptorless Dehydrogenation/Hydrogenation of N-Substituted and Unsubstituted Heterocycles Enabled by a Polymer-Cross-Linking Bisphosphine
Zhang, Deliang,Iwai, Tomohiro,Sawamura, Masaya
supporting information, p. 5240 - 5245 (2020/07/03)
The polystyrene-cross-linking bisphosphine ligand PS-DPPBz was effective for the Ir-catalyzed reversible acceptorless dehydrogenation/hydrogenation of N-heterocycles. Notably, this protocol is applicable to the dehydrogenation of N-substituted indoline derivatives with various N-substituents with different electronic and steric natures. A reaction pathway involving oxidative addition of an N-adjacent C(sp3)-H bond to a bisphosphine-coordinated Ir(I) center is proposed for the dehydrogenation of N-substituted substrates.
BENZODIAZEPINE DERIVATIVES AND THEIR USE AS ANTAGONISTS OF CHOLECYSTOKININ AND/OR GASTRIN RECEPTORS
-
, (2008/06/13)
-
