49672-05-1 Usage
General Description
Methyl 2-(1H-benzoimidazol-2-yl)acetate is a compound that consists of a methyl group attached to a 2-(1H-benzoimidazol-2-yl)acetate group. It is a synthetic chemical that is commonly used in organic synthesis and pharmaceutical research. methyl 2-(1H-benzoimidazol-2-yl)acetate has potential applications in the development of new pharmaceutical drugs due to its ability to interact with biological systems and exhibit specific biological activities. Its precise chemical structure and properties make it a valuable tool for scientists and researchers working on drug discovery and development. Additionally, its stability and reactivity make it suitable for various synthetic processes in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 49672-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,7 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 49672-05:
(7*4)+(6*9)+(5*6)+(4*7)+(3*2)+(2*0)+(1*5)=151
151 % 10 = 1
So 49672-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O2/c1-14-10(13)6-9-11-7-4-2-3-5-8(7)12-9/h2-5H,6H2,1H3,(H,11,12)
49672-05-1Relevant articles and documents
A new route to pyrimido [1,6-a] benzimidazoles : Reactivity of activated 2-benzimidazoles with N-Acyl imidates as β-dielectrophiles under microwave irradiation
Rahmouni, Mustapha,Derdour, Aicha,Bazureau, Jean Pierre,Hamelin, Jack
, p. 4563 - 4564 (1994)
Activated 2-benzimidazoles react with a variety of N-Acyl imidates under microwave irradiation in open vessels to give the corresponding pyrimido [1,6-a] benzimidazoles.
Synthesis of β-enamino acid and heteroaryl acetic acid derivatives by Pd-catalyzed carbonylation of α-chloroimines and 2-chloromethyl aza-heterocycles
Perrone, Serena,Capua, Martina,Cannazza, Giuseppe,Salomone, Antonio,Troisi, Luigino
supporting information, p. 1421 - 1424 (2016/03/12)
β-Enamino esters or amides can be synthesized in a single step by a carbonylative coupling of α-chloroimines with alcohols or amines under Pd-catalysis. The methodology has been also applied to the preparation of heteroaryl acetic acid derivatives starting from chloromethyl heteroaromatic rings containing a C-N double bond. The in situ generation of a β-imino acylpalladium species has been proposed as a key step for the process.
