7114-78-5 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Dimethyl-1(2H)-isoquinolone is used as a key intermediate in the synthesis of various drugs. Its role in drug development is crucial due to its ability to form complex molecular structures that can be tailored for specific therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-Dimethyl-1(2H)-isoquinolone is used as a precursor in the production of pesticides and other agricultural chemicals. Its chemical properties allow for the creation of compounds that can effectively control pests and diseases in crops.
Used in Fine Chemicals Industry:
2,3-Dimethyl-1(2H)-isoquinolone is also utilized in the synthesis of fine chemicals, which are specialty chemicals used in various applications such as fragrances, dyes, and other industrial processes. Its versatility in chemical reactions contributes to the development of innovative products in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 7114-78-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7114-78:
(6*7)+(5*1)+(4*1)+(3*4)+(2*7)+(1*8)=85
85 % 10 = 5
So 7114-78-5 is a valid CAS Registry Number.
7114-78-5Relevant academic research and scientific papers
HETEROCYCLIC SYNTHESIS VIA THALLATION AND SUBSEQUENT PALLADIUM-PROMOTED OLEFINATION
Larock, R.C.,Liu, C.-L.,Lau, H. H.,Varaprath, S.
, p. 4459 - 4462 (2007/10/02)
The thallation and subsequent palladium-promoted olefination of p-tolylacetic acid, N-methylbenzamide, benzamide and acetanilide provides a novel new route to a variety of important oxygen and nitrogen heterocycles.
Recyclization of 3-Alkyl- and 1,3-Dialkylisoquinolinium Salts to Naphthylamines
Kost, A. N.,Terenin, V. I.,Yudin, L. G.,Sagitullin, R. S.
, p. 965 - 969 (2007/10/02)
3-Methyl- and 3-benzylisoquinolinium salts undergo rearrangement to 2-alkylaminonaphthalenes under the influence of alcohol solutions of alkylamines.The rearrangement of 1,3-dimethyl- and 1-methyl-3-benzylisoquinolinium salts leads to both 1- and 2-alkylaminonaphthalenes with predominance of the former.
