130670-12-1 Usage
General Description
The chemical "(4-Methyl-2-phenylpyrimidin-5-yl)-acetic acid methyl ester" is an organic compound with the molecular formula C14H14N2O2. It is a methyl ester derivative of the compound (4-Methyl-2-phenylpyrimidin-5-yl)-acetic acid, and is used in a variety of chemical and pharmaceutical applications. (4-Methyl-2-phenylpyrimidin-5-yl)-acetic acid methyl ester is of interest to researchers and scientists due to its potential medicinal and biological properties, and its structure and properties make it a candidate for further study in drug development and related fields. It may have potential uses in the development of new medications and treatments, and its properties make it an important compound for research and experimentation in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 130670-12-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,7 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130670-12:
(8*1)+(7*3)+(6*0)+(5*6)+(4*7)+(3*0)+(2*1)+(1*2)=91
91 % 10 = 1
So 130670-12-1 is a valid CAS Registry Number.
130670-12-1Relevant articles and documents
Reaction of Methyl (E)-2-Phenyl-1-azirine-3-acrylates with Hydrazines and Amidines. Synthetic and Mechanistic Implications
Kascheres, Albert,Oliveira, Cecilia M. A.,Azevedo, Mariangela . M. de,Nobre, Cintia M. S.
, p. 7 - 9 (2007/10/02)
1-Azirines 2a-b react with hydrazine in methanol to produce hexahydropyrrolopyrazol-5-ones 3a-b.The process is suggested to involve intramolecular interception of an unstable 4-aminopyrazoline intermediate resulting from C=N bond cleavage.Reaction of 2a with phenylhydrazine similarly affords 3c.In dimethyl sulfoxide, on the other hand, formamidine, guanidine, and hydrazine afford imidazole 4, pyrimidines 5a-b, amino-s-triazine 6, or triazole 9 as a consequence of C-C bond cleavage in aziridine intermediate 8.The intermediacy of tautomers is proposed to account for the diversity of products in this case.