6969-98-8 Usage
Description
[2-(dimethylaminomethyl)phenyl]-diphenyl-methanol is a complex chemical compound featuring a diphenylmethane core with a [2-(dimethylaminomethyl)phenyl] group attached. [2-(dimethylaminomethyl)phenyl]-diphenyl-methanol is recognized for its potential applications as a fluorescent dye and a pharmaceutical intermediate, attributed to its aromatic and hydroxyl groups. The presence of the dimethylaminomethyl and phenyl groups indicates that it may have unique chemical properties and reactivity, which could be of interest to researchers and chemists in various scientific fields. Given its intricate structure and potential uses, further exploration into its properties and applications is necessary.
Uses
Used in Pharmaceutical Industry:
[2-(dimethylaminomethyl)phenyl]-diphenyl-methanol is used as a pharmaceutical intermediate for its potential role in the development of new drugs. [2-(dimethylaminomethyl)phenyl]-diphenyl-methanol's unique structure and reactivity may allow for the creation of novel medications with specific therapeutic properties.
Used in Chemical Research:
[2-(dimethylaminomethyl)phenyl]-diphenyl-methanol serves as a subject of interest in chemical research due to its complex structure and the potential for unique chemical properties. Researchers may use it to study various aspects of organic chemistry, including synthesis, reactivity, and the development of new methodologies.
Used in Dye Industry:
[2-(dimethylaminomethyl)phenyl]-diphenyl-methanol is used as a fluorescent dye in the dye industry, taking advantage of its aromatic and hydroxyl groups to create dyes with specific optical properties for various applications, such as in the production of materials with specialized optical characteristics.
Used in Organic Synthesis:
[2-(dimethylaminomethyl)phenyl]-diphenyl-methanol is employed in organic synthesis to create other organic compounds. Its unique structure and reactivity make it a valuable building block for the development of new chemical entities with potential applications in various industries, including pharmaceuticals, materials science, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 6969-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6969-98:
(6*6)+(5*9)+(4*6)+(3*9)+(2*9)+(1*8)=158
158 % 10 = 8
So 6969-98-8 is a valid CAS Registry Number.
InChI:InChI=1/C22H23NO/c1-23(2)17-18-11-9-10-16-21(18)22(24,19-12-5-3-6-13-19)20-14-7-4-8-15-20/h3-16,24H,17H2,1-2H3
6969-98-8Relevant articles and documents
'Counter-intuitive' regioselectivity, subtle steric and solvation effects in lithiation of cyclic tertiary aralkylamines
Kessar, Satinder V.,Singh, Paramjit,Singh, Kamal Nain,Venugopalan,Kaur, Amarjit,Mahendru, Manu,Kapoor, Rajiv
, p. 6753 - 6755 (2007/10/03)
Lithiation of a series of cyclic aralkyl tertiary amines with sec-BuLi in various solvents has been studied. There is a subtle sensitivity to steric factors and lithium coordinating solvents/additives have an adverse effect. ortho-Lithiation is observed only in the case of an eight-membered cyclic amine and the ease of benzylic lithiation with respect to nitrogen is in the surprising order γ > β ? α, δ. These observations are discussed in the context of nitrogen coordination promoted lithiation.