2215-78-3 Usage
Description
(4-Phenoxyphenyl)methanol, also known as 4-hydroxyphenyl phenylmethanol, is an organic compound with the chemical formula C13H12O2. It is a colorless crystalline solid that is soluble in organic solvents. (4-PHENOXYPHENYL)METHANOL is characterized by the presence of a phenolic hydroxyl group and a benzylic hydroxyl group, which contribute to its unique chemical properties and reactivity.
Uses
Used in Organic Synthesis:
(4-Phenoxyphenyl)methanol is used as a reactant and reagent in various organic reactions and synthesis processes. Its unique chemical structure allows it to participate in a wide range of reactions, making it a versatile building block for the synthesis of more complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4-phenoxyphenyl)methanol is used as an intermediate in the synthesis of various drugs and drug candidates. Its ability to participate in a variety of organic reactions makes it a valuable component in the development of new medications with potential therapeutic benefits.
Used in Chemical Research:
(4-Phenoxyphenyl)methanol is also used in chemical research as a model compound to study various organic reactions and mechanisms. Its unique structure and reactivity provide valuable insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2215-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2215-78:
(6*2)+(5*2)+(4*1)+(3*5)+(2*7)+(1*8)=63
63 % 10 = 3
So 2215-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c14-10-11-6-8-13(9-7-11)15-12-4-2-1-3-5-12/h1-9,14H,10H2
2215-78-3Relevant articles and documents
Graczyk et al.
, p. 7333,7338 (1978)
PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS
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Page/Page column 305, (2020/10/18)
This disclosure provides pharmaceutical compounds to treat medical disorders, such as complement-mediated disorders, including complement Cl -mediated disorders.
Preparation method of 4-benzyloxybenzyl alcohol
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Paragraph 0017-0020, (2018/03/25)
The invention relates to a preparation method of 4-benzyloxybenzyl alcohol. The preparation method comprises the specific steps: A, adding a proper amount of dimethylformamide, p-fluorobenzaldehyde, phenol, inorganic alkali and cuprous salt in a reaction kettle, stirring to rise the temperature, controlling the temperature at 100 DEG C to 150 DEG C and carrying out a reaction, after completion ofthe reaction, cooling to room temperature, filtering to remove inorganic salt, then recycling dimethylformamide, adding the obtained 4-benzyloxybenzaldehyde in methanol and dissolving; and B, adding the methanol solution of 4-benzyloxybenzaldehyde and a catalyst into a pressure kettle, controlling the temperature at 50 DEG C to 70 DEG C, introducing hydrogen and carrying out a reaction, keeping the hydrogen pressure at 5 kg/cm or more, after completion of the reaction, cooling to room temperature, filtering to remove the catalyst under anaerobic conditions, then recycling methanol, carryingout cooling crystallization of the remaining product, and thus obtaining 4-benzyloxybenzyl alcohol. The preparation method of 4-benzyloxybenzyl alcohol is simple in route and high in yield.
