26791-93-5 Usage
General Description
Methyl 4,5-dimethoxy-2-nitrobenzoate is a chemical compound with the molecular formula C10H11NO6. It is a nitrobenzoate derivative, which means it contains a nitro group (-NO2) attached to a benzoate molecule. Methyl 4,5-dimethoxy-2-nitrobenzoate is commonly used in organic synthesis and pharmaceutical research due to its potential pharmacological properties. The presence of methoxy and nitro groups on the benzene ring makes this compound an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used as a reagent in organic reactions and as a building block for creating more complex chemical structures. However, it is important to handle and use this compound with caution as it can pose health hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 26791-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,7,9 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26791-93:
(7*2)+(6*6)+(5*7)+(4*9)+(3*1)+(2*9)+(1*3)=145
145 % 10 = 5
So 26791-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO6/c1-15-8-4-6(10(12)17-3)7(11(13)14)5-9(8)16-2/h4-5H,1-3H3
26791-93-5Relevant articles and documents
OXOACRIDINYL ACETIC ACID DERIVATIVES AND METHODS OF USE
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Page/Page column 99-100, (2020/11/30)
Compounds of Formulae I, II, their pharmaceutically acceptable salts or esters thereof capable of binding to and modulating the activity of a stimulator of interferon genes (STING) protein are provided. Methods involving compounds of Formulae I or II as effective modulators of STING are also provided.
Method of Synthesizing 6,7-Substituted 4-Anilino Quinazoline
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Page/Page column 6, (2010/11/03)
A method of synthesizing 6,7-substituted 4-anilino quinazoline employs 3,4-substituted benzoic acid as an initial reactant, and the 6,7-substituted 4-anilino quinazoline is obtained by an esterifying step, a nitrating step, a reducing step, a cyclizing step, and an one-pot reaction. In the above method, the initial reactant has low cost and yield. of the 6,7-substituted 4-anilino quinazoline is high, therefore, production cost can be reduced effectively, and competitive power of the product of the 6,7-substituted 4-anilino quinazoline can be improved.
An expeditious, practical large scale synthesis of 4-amino-2-chloro-6,7- dimethoxyquinazoline
Kumaraswamy,Jena, Nivedita,Sastry,Kumar, B. Ashok
, p. 341 - 345 (2007/10/03)
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