21523-62-6 Usage
General Description
2,3-Dimethyl-1 H-indole-5-carboxylic acid ethyl ester is a chemical compound with the molecular formula C14H15NO2. It is a white to off-white crystalline solid with a molecular weight of 229.27 g/mol. 2,3-DIMETHYL-1 H-INDOLE-5-CARBOXYLIC ACID ETHYL ESTER is commonly used in organic synthesis and the pharmaceutical industry as a building block for the preparation of various pharmaceuticals and agrochemicals. It is also utilized as a reagent in the synthesis of novel compounds with potential biological activities. Additionally, it may have applications in the field of material science, particularly in the development of functional materials and polymers.
Check Digit Verification of cas no
The CAS Registry Mumber 21523-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,2 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21523-62:
(7*2)+(6*1)+(5*5)+(4*2)+(3*3)+(2*6)+(1*2)=76
76 % 10 = 6
So 21523-62-6 is a valid CAS Registry Number.
21523-62-6Relevant articles and documents
PPARG MODULATORS FOR TREATMENT OF OSTEOPOROSIS
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Page/Page column 241; 242, (2015/11/09)
The invention provides methods of treatment of a progressive bone disease, such as osteoporosis, Paget's Disease, multiple myeloma, or hyperparathyroidism, comprising administration of an effective amount of a non-agonist PPARG modulator to a patient afflicted with the disease.
Fischer indole synthesis with organozinc reagents
Haag, Benjamin A.,Zhang, Zhi-Guang,Li, Jin-Shan,Knochel, Paul
supporting information; experimental part, p. 9513 - 9516 (2011/02/24)
Updated classic: Primary and secondary alkylzinc reagents add to various aryldiazonium salts leading regioselectively to polyfunctional indoles by means of a [3,3]-sigmatropic shift and subsequent aromatization. This organometallic variation of the Fischer indole synthesis tolerates a wide range of functional groups and displays absolute regioselectivity. Copyright