6624-01-7 Usage
Uses
Used in Pharmaceutical Industry:
[2-(diphenylmethyl)phenyl]methanol is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and medications. Its unique structure allows for the creation of a diverse range of compounds with potential therapeutic applications.
Used in Fragrance Industry:
In the fragrance industry, [2-(diphenylmethyl)phenyl]methanol is used as a component in the creation of various scents. Its chemical properties make it suitable for use in the formulation of perfumes, colognes, and other aromatic products, enhancing their overall quality and appeal.
Used in Chemical Industry:
[2-(diphenylmethyl)phenyl]methanol is also utilized in the chemical industry as a key building block for the synthesis of a wide array of organic compounds. Its versatility in chemical reactions enables the production of various specialty chemicals that serve different purposes and applications across multiple industries.
Production Methods:
[2-(diphenylmethyl)phenyl]methanol can be prepared through different methods, including the reduction of benzophenone using sodium borohydride or the Grignard reaction of benzophenone with phenylmagnesium bromide, followed by acidic hydrolysis. These methods allow for the efficient and effective synthesis of the compound, making it accessible for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6624-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6624-01:
(6*6)+(5*6)+(4*2)+(3*4)+(2*0)+(1*1)=87
87 % 10 = 7
So 6624-01-7 is a valid CAS Registry Number.
6624-01-7Relevant academic research and scientific papers
Electron-transfer-induced reductive cleavage of phthalans: Reactivity and synthetic applications
Azzena, Ugo,Demartis, Salvatore,Melloni, Giovanni
, p. 4913 - 4919 (2007/10/03)
The behavior of phthalan (1a) was investigated under conditions of electron transfer from alkali metals in aprotic solvents. Reaction with lithium in the presence of a catalytic amount of naphthalene in THF led to the reductive cleavage of an arylmethyl carbon-oxygen bond, with formation of a stable dilithium compound. Trapping of this intermediate with several electrophiles (alkyl halides, carbonyl derivatives, CO2) was successful. The extension of this procedure to several substituted phthalans (1b-i) was investigated, and the regiochemistry as well as the synthetic usefulness of these reactions are discussed.
