219834-81-8 Usage
General Description
The chemical 1H-Pyrrolo[3,2-c]pyridine-1-carboxylic acid,2,3-dihydro-1,1-diemthylethyl ester is an organic compound with the molecular formula C14H17NO3. It is commonly used as a reagent in chemical synthesis and pharmaceutical research. 1H-Pyrrolo[3,2-c]pyridine-1-carboxylic acid,2,3-dihydro-1,1-diemthylethyl ester is an ester derivative of carboxylic acid and has two methyl groups attached to the nitrogen atom. It is a colorless to pale yellow liquid with a fruity odor, and it is insoluble in water but soluble in organic solvents. This chemical is often used in the production of pharmaceutical drugs and agrochemicals, as well as in the synthesis of other organic compounds. It is important to handle this substance with care, as it can be hazardous if not used properly.
Check Digit Verification of cas no
The CAS Registry Mumber 219834-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,8,3 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 219834-81:
(8*2)+(7*1)+(6*9)+(5*8)+(4*3)+(3*4)+(2*8)+(1*1)=158
158 % 10 = 8
So 219834-81-8 is a valid CAS Registry Number.
219834-81-8Relevant articles and documents
HETEROCYCLIC COMPOUNDS AND THEIR USE FOR TREATMENT OF HELMINTHIC INFECTIONS AND DISEASES
-
, (2020/11/03)
Provided herein are Heterocyclic compounds of formula (I): and pharmaceutically acceptable salts, tautomers, isotopologues, or stereoisomers thereof, wherein W, X, Y, R1, R2, and RN are as defined herein, compositions comprising an effective amount of a Heterocyclic Compound, and methods for treating or preventing animal and human filarial worm infections and diseases.
Synthesis of atropisomeric analogues of DMAP
Spivey, Alan C.,Fekner, Tomasz,Adams, Harry
, p. 8919 - 8922 (2007/10/03)
A method for the preparation of 7-aryl derivatives of N-methyl-5- azaindolinee involving Suzuki cross-coupling is described. Certain biaryls prepared in this manner exhibit atropisomerism. In particular, azaindoline 11 is shown to be configurationally sta
