110102-86-8 Usage
Description
5-Amino-4-chloro-2-methylphenol is an organic compound characterized by its unique chemical structure, which features an amino group at the 5th position, a chlorine atom at the 4th position, and a methyl group at the 2nd position on a phenol ring. 5-Amino-4-chloro-2-methylphenol is known for its versatile applications in various industries due to its distinct chemical properties.
Uses
Used in Pharmaceutical Industry:
5-Amino-4-chloro-2-methylphenol is used as a reagent for the synthesis of biospecific compounds, which are designed to interact with specific biological targets. These compounds exhibit biological activity, making them valuable in the development of pharmaceuticals for various therapeutic applications.
Used in Contraceptive Development:
In the contraceptive industry, 5-Amino-4-chloro-2-methylphenol is utilized for its spermicidal activity. This property makes it a potential candidate for the development of new contraceptive methods, offering an alternative to existing options and potentially improving reproductive health outcomes.
Used in Chemical Synthesis:
5-Amino-4-chloro-2-methylphenol is also used as a building block in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with different properties and applications, making it a valuable asset in the field of chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 110102-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,0 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110102-86:
(8*1)+(7*1)+(6*0)+(5*1)+(4*0)+(3*2)+(2*8)+(1*6)=48
48 % 10 = 8
So 110102-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H8ClNO/c1-4-2-5(8)6(9)3-7(4)10/h2-3,10H,9H2,1H3
110102-86-8Relevant articles and documents
Enantioselective Vanadium-Catalyzed Oxidative Coupling: Development and Mechanistic Insights
Kang, Houng,Herling, Madison R.,Niederer, Kyle A.,Lee, Young Eun,Vasu Govardhana Reddy, Peddiahgari,Dey, Sangeeta,Allen, Scott E.,Sung, Paul,Hewitt, Kirsten,Torruellas, Carilyn,Kim, Gina J.,Kozlowski, Marisa C.
, p. 14362 - 14384 (2018/11/23)
The evolution of a more reactive chiral vanadium catalyst for enantioselective oxidative coupling of phenols is reported, ultimately resulting in a simple monomeric vanadium species combined with a Br?nsted or Lewis acid additive. The resultant vanadium complex is found to effect the asymmetric oxidative ortho-ortho coupling of simple phenols and 2-hydroxycarbazoles with good to excellent levels of enantioselectivity. Experimental and quantum mechanical studies of the mechanism indicate that the additives aggregate the vanadium monomers. In addition, a singlet to triplet crossover is implicated prior to carbon-carbon bond formation. The two lowest energy diastereomeric transition states leading to the enantiomeric products differ substantially with the path to the minor enantiomer involving greater torsional strain between the two phenol moieties.