76-82-4 Usage
Description
(4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol, also known as Bis-amino-phenyl-methanol or 4-(4-(4-aminophenyl)-3-methylphenylamino)benzyl alcohol, is a bisphenol derivative with a complex molecular structure. It features two amino groups and a benzyl alcohol moiety, which contribute to its unique properties and reactivity. This chemical compound holds potential for applications in organic synthesis, pharmaceuticals, polymer production, and other industrial processes.
Uses
Used in Organic Synthesis:
(4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol is used as a key intermediate for the synthesis of various organic compounds due to its reactive amino and benzyl alcohol groups, which can participate in a range of chemical reactions to form diverse products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol is used as a building block for the development of new drugs. Its unique structure allows it to be a potential candidate for the creation of molecules with specific therapeutic properties, such as antimicrobial, antiviral, or anticancer agents.
Used in Polymer Production:
(4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol is utilized as a monomer in the production of polymers. Its ability to form covalent bonds with other monomers makes it a valuable component in the synthesis of polymers with tailored properties for various applications, such as coatings, adhesives, or plastics.
Used in Industrial Processes:
(4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol may also find use in other industrial processes where its unique structure and reactivity can be leveraged to improve or enable new methods of production, potentially leading to more efficient or sustainable processes.
Further research is necessary to fully explore the properties and potential uses of (4-amino-3-methyl-phenyl)-bis(4-aminophenyl)methanol, as its complex structure offers a wide range of possibilities in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 76-82-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76-82:
(4*7)+(3*6)+(2*8)+(1*2)=64
64 % 10 = 4
So 76-82-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H21N3O/c1-13-12-16(6-11-19(13)23)20(24,14-2-7-17(21)8-3-14)15-4-9-18(22)10-5-15/h2-12,24H,21-23H2,1H3
76-82-4Relevant articles and documents
Kinetics of reduction of triaminotolyldiphenylmethane chloride (rosaniline hydrochloride) by hydroxide ions in aqueous medium
Iyun,Peters,Babutunde
, p. 967 - 969 (2007/10/03)
Kinetics and mechanism of reduction of rosaniline hydrochloride (RH) by hydroxide ions have been studied in aqueous medium at 30°C at ionic strength of 1.0 mol dm-3 (NaCl). The reduction follows a second order kinetics and it conforms to the rate law: -d/dt [RH] = k2 [RH][OH-] and k2 is found to be 1.84 ± 0.04 × 102 mol dm-3 min-1. The rate of reaction is not sensitive to changes in dielectric constant of the medium and free radicals have not been detected in the reaction. The rate of reaction decreased with increase in ionic strength. The results from our spectroscopic investigations and Michaelis-Menten analysis do not show any evidence for an intermediate of significant stability. The outersphere mechanism is, therefore, postulated for this reaction.
