6538-32-5 Usage
Uses
Used in Organic Synthesis:
Benzene-1,2-diylbis(diphenylmethanol) is used as a building block for the synthesis of various organic compounds and materials due to its high reactivity and versatility.
Used in Polymer Production:
benzene-1,2-diylbis(diphenylmethanol) is used as a key component in the production of polymers, contributing to the development of materials with specific properties for diverse applications.
Used in Pharmaceutical Industry:
Benzene-1,2-diylbis(diphenylmethanol) is utilized in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medicines.
Used in Agrochemical Production:
It serves as an important intermediate in the production of agrochemicals, helping to create effective solutions for agricultural needs.
Used as a Crosslinking Agent:
In the production of resins and adhesives, benzene-1,2-diylbis(diphenylmethanol) is used as a crosslinking agent, enhancing the strength and durability of these materials.
Used in Specialty Chemicals Synthesis:
benzene-1,2-diylbis(diphenylmethanol) is also used in the synthesis of dyes, pigments, and other specialty chemicals, contributing to the creation of a wide range of products across various industries.
Safety Note:
It is important to handle benzene-1,2-diylbis(diphenylmethanol) with care, as it is toxic and can pose health risks if not properly managed. Proper safety measures should be taken to minimize exposure and ensure safe handling during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6538-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6538-32:
(6*6)+(5*5)+(4*3)+(3*8)+(2*3)+(1*2)=105
105 % 10 = 5
So 6538-32-5 is a valid CAS Registry Number.
6538-32-5Relevant academic research and scientific papers
Azobenzene-tethered bis(trityl alcohol) as a photoswitchable cooperative acid catalyst for Morita-Baylis-Hillman reactions
Imahori, Tatsushi,Yamaguchi, Ryo,Kurihara, Seiji
supporting information; experimental part, p. 10802 - 10807 (2012/09/22)
Incorporation of an azobenzene core into tethered bis(trityl alcohol) allows the photoswitchable arrangement of the two trityl alcohol units through photoisomerization of azobenzene. The differently arranged trityl alcohol units change their cooperative function to reflect the positional relationships, and thus, the activity as a cooperative acid can be controlled by light stimuli (see figure). Copyright
New Hosts Bearing Two Triphenylcarbinol Groups and Crystal Structures of Their Acetone Inclusion Compounds
Toda, Fumio,Kai, Akira,Toyotaka, Ritsuji,Yip, Wai-Hing,Mak, Thomas C. W.
, p. 1921 - 1924 (2007/10/02)
New hosts, m- and p-bis(diphenylhydroxymethyl)benzene and 2,2'-bis(diphenylhydroxymethyl)-1,1'-diphenyl, were found to exhibit high and selective inclusion tendencies toward a wide variety of guest compounds.Crystal structures of two representative acetone complexes were determined.