123239-65-6 Usage
Uses
Used in Pharmaceutical Industry:
(4-Methoxynaphthalen-2-yl)(phenyl)Methanol is used as an intermediate for the synthesis of various pharmaceutical compounds. Its aromatic and phenolic properties contribute to its utility in creating a range of medicinal products.
Used in Agrochemical Industry:
In the agrochemical sector, (4-Methoxynaphthalen-2-yl)(phenyl)Methanol is utilized as a building block for the development of different agrochemicals, such as pesticides and fertilizers, due to its chemical reactivity and structural properties.
Used in Specialty Chemicals Production:
(4-Methoxynaphthalen-2-yl)(phenyl)Methanol is also employed in the production of specialty chemicals, which are tailored for specific industries and applications, taking advantage of its unique chemical characteristics.
Precautionary Note:
It is crucial to handle (4-Methoxynaphthalen-2-yl)(phenyl)Methanol with care, as it may pose health risks if ingested, inhaled, or absorbed through the skin. Additionally, it has the potential to cause eye and skin irritation. Appropriate safety measures should be taken during its use and storage to minimize potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 123239-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,3 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 123239-65:
(8*1)+(7*2)+(6*3)+(5*2)+(4*3)+(3*9)+(2*6)+(1*5)=106
106 % 10 = 6
So 123239-65-6 is a valid CAS Registry Number.
123239-65-6Relevant academic research and scientific papers
2-Substituted-1-naphthols as potent 5-lipoxygenase inhibitors with topical antiinflammatory activity
Batt,Maynard,Petraitis,Shaw,Galbraith,Harris
, p. 360 - 370 (2007/10/02)
The synthesis, biological evaluation, and structure-activity relationships of a series of 1-naphthols bearing carbon substituents at the 2-position are described. These compounds are potent inhibitors of the 5-lipoxygenase from RBL-1 cells and also inhibi
