1453-50-5 Usage
Description
4-(2,5-DIMETHYLPHENYL)BUTYRIC ACID, also known as DMBA, is a chemical compound with the molecular formula C12H16O2. It is a derivative of butyric acid and contains a 2,5-dimethylphenyl group. DMBA is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. It is also used as a chiral auxiliary in asymmetric synthesis reactions. Additionally, DMBA has been studied for its potential role in the treatment of various medical conditions, including neurological disorders and cancer. 4-(2,5-DIMETHYLPHENYL)BUTYRIC ACID is considered to have low toxicity and is not known to pose significant health risks when handled and used properly.
Uses
Used in Pharmaceutical Industry:
4-(2,5-DIMETHYLPHENYL)BUTYRIC ACID is used as a precursor in the synthesis of various pharmaceuticals and organic compounds for the development of new drugs and medications.
Used in Chemical Industry:
4-(2,5-DIMETHYLPHENYL)BUTYRIC ACID is used as a chiral auxiliary in asymmetric synthesis reactions to facilitate the production of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical applications.
Used in Medical Research:
4-(2,5-DIMETHYLPHENYL)BUTYRIC ACID is used in the study of its potential role in the treatment of various medical conditions, including neurological disorders and cancer, to explore its therapeutic properties and possible applications in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 1453-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,5 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1453-50:
(6*1)+(5*4)+(4*5)+(3*3)+(2*5)+(1*0)=65
65 % 10 = 5
So 1453-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c9-7(5-1-2-5)8-6-3-4-6/h5-6H,1-4H2,(H,8,9)
1453-50-5Relevant articles and documents
Synthesis of N-alkylimidazolium salts and their utility as solvents in the Beckmann rearrangement
Elango, Kandasamy,Srirambalaji, Renganathan,Anantharaman, Ganapathi
, p. 9059 - 9062 (2008/03/18)
Six different room temperature ionic liquids (RTILs) based on N-methyl or N-isopropyl imidazolium cations with counteranions, such as BF4-, PF6-, and OTf-, have been synthesized by exchanging the counteranions of the corresponding N-methyl or N-isopropylimidazolium bromides using appropriate salts such as NH4BF4, KPF6, and AgOTf. Catalytic amounts of these ionic liquids (ILs) have been used as the reaction medium for the Beckmann rearrangement of oximes to amides in the presence of PCl5. A moderate to good conversion of oximes to amides in all the six ILs was observed.
TRIAZOLE DERIVATIVES AS INHIBITORS OF 11-BETA HYDROXYSTEROID DEHYDROGENASE-1
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Page 33, (2008/06/13)
Triazole derivatives of structural formula I are selective inhibitors of the 11β-hydroxysteroid dehydrogenase-1. The compounds are useful for the treatment of diabetes, such as noninsulin-dependent diabetes (NIDDM), hyperglycemia, obesity, insulin resistance, dyslipidemia, hyperlipidemia, hypertension, Metabolic Syndrome, and other symptoms associated with NIDDM.