29921-41-3 Usage
General Description
2-Chlorodiphenylmethane, also known as chlorodiphenylmethane or benzhydrol chloride, is an organic compound with the molecular formula C13H11Cl. It is a colorless solid that is sparingly soluble in water but more soluble in organic solvents. This chemical is primarily used as an intermediate in the production of other chemicals, such as pharmaceuticals and agrochemicals. It is also used as a reactant in organic synthesis and as a building block for the creation of other organic compounds. 2-Chlorodiphenylmethane is classified as a Hazardous Substance according to the Environmental Protection Agency (EPA) and should be handled and disposed of with proper safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 29921-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,2 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29921-41:
(7*2)+(6*9)+(5*9)+(4*2)+(3*1)+(2*4)+(1*1)=133
133 % 10 = 3
So 29921-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H11Cl/c14-13-9-5-4-8-12(13)10-11-6-2-1-3-7-11/h1-9H,10H2
29921-41-3Relevant articles and documents
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Hassan,M.,Yousif,G.
, p. 459 - 462 (1968)
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Controlled Access to C1-Symmetrical Cyclotriveratrylenes (CTVs) by Using a Sequential Barluenga Boronic Coupling (BBC) Approach
Cailly, Thomas,Dubost, Emmanuelle,Fabis, Frédéric,Fossé, Pierre,Vigier, Clément
supporting information, p. 3756 - 3761 (2021/07/14)
We describe here a controlled approach to C1-symmetrical cyclotriveratrylenes (CTVs). In this approach dimers are synthesized through Barluenga boronic coupling (BBC) and after borylation, the last aromatic ring is introduced by a second BBC. After functional transformations of the trimers, the CTVs are formed using intramolecular SEAr. (Figure presented.).
Carbonyl and olefin hydrosilylation mediated by an air-stable phosphorus(iii) dication under mild conditions
Andrews, Ryan J.,Chitnis, Saurabh S.,Stephan, Douglas W.
supporting information, p. 5599 - 5602 (2019/05/21)
The readily-accessible, air-stable Lewis acid [(terpy)PPh][B(C6F5)4]21 is shown to mediate the hydrosilylation of aldehydes, ketones, and olefins. The utility and mechanism of these hydrosilylations are considered.
