247575-34-4 Usage
Uses
Used in Pharmaceutical Industry:
(3-bromo-2,5-dimethylphenyl)methanol is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structure of various drugs, enhancing their therapeutic properties and effectiveness.
Used in Organic Compounds Synthesis:
(3-bromo-2,5-dimethylphenyl)methanol is used as a building block in the production of various industrial chemicals for its versatility in forming different chemical structures and contributing to the development of new compounds with specific applications.
Used in Chemical Research:
(3-bromo-2,5-dimethylphenyl)methanol is used as a research compound in the field of organic chemistry for its potential to be modified and studied for new reactions and properties, contributing to the advancement of chemical knowledge and innovation.
It is important to handle (3-bromo-2,5-dimethylphenyl)methanol with care, as it may cause irritation to the skin, eyes, and respiratory system if not handled properly. Additionally, it has the potential to be harmful if ingested or inhaled in large quantities.
Check Digit Verification of cas no
The CAS Registry Mumber 247575-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,7,5,7 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 247575-34:
(8*2)+(7*4)+(6*7)+(5*5)+(4*7)+(3*5)+(2*3)+(1*4)=164
164 % 10 = 4
So 247575-34-4 is a valid CAS Registry Number.
247575-34-4Relevant academic research and scientific papers
INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL
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Page/Page column 91, (2010/11/18)
This invention relates to compounds having structural Formula I: and pharmaceutically acceptable salts thereof which are inhibitors of the Renal Outer Medullary Potassium (ROMK) channel (Kir1.1). The compounds of Formula I are useful as diuretics and natriuretics and therefore are useful for the therapy and prophylaxis of disorders resulting from excessive salt and water retention, including cardiovascular diseases such as hypertension and chronic and acute heart failure
Synthesis, reactions, and structural and NMR features of [2.2]metacyclophane monoenes and their tricarbonylchromium and cyclopentadienyliron(+) complexes
Mitchell, Reginald H.,Zhang, Limin
, p. 7140 - 7152 (2007/10/03)
8,16-Dimethyl-, 5,8,13,16-tetramethyl-, and 4,6,8,12,14,16- hexamethyl[2.2]metacyclophanene have been synthesized from the corresponding methyl-substituted 3-thia[3.2]metacyclophane precursors via a Wittig rearrangement-Hofmann elimination procedure. Simp
