60811-17-8 Usage
Description
5-Bromo-2-chloroaniline is an organic compound characterized by its tan solid appearance. It is a significant intermediate in the synthesis of various organic compounds, particularly in the agrochemical, pharmaceutical, and dyestuff industries.
Uses
Used in Agrochemical Industry:
5-Bromo-2-chloroaniline is used as an important raw material and intermediate for the development of agrochemicals. It plays a crucial role in the production of pesticides and other chemicals that help protect crops from pests and diseases, ensuring a stable food supply.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 5-bromo-2-chloroaniline serves as a key intermediate in the synthesis of various drugs. Its unique chemical properties allow it to be incorporated into the molecular structures of medications, potentially enhancing their efficacy and targeting specific health conditions.
Used in Dyestuff Industry:
5-Bromo-2-chloroaniline is also utilized in the dyestuff industry as a vital component in the creation of synthetic dyes. These dyes are used in a wide range of applications, from textiles and fabrics to various industrial processes, providing vibrant colors and enhancing the visual appeal of products.
Check Digit Verification of cas no
The CAS Registry Mumber 60811-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,1 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60811-17:
(7*6)+(6*0)+(5*8)+(4*1)+(3*1)+(2*1)+(1*7)=98
98 % 10 = 8
So 60811-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrClN/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
60811-17-8Relevant articles and documents
Catalyst-Controlled Regioselective Chlorination of Phenols and Anilines through a Lewis Basic Selenoether Catalyst
Dinh, Andrew N.,Maddox, Sean M.,Vaidya, Sagar D.,Saputra, Mirza A.,Nalbandian, Christopher J.,Gustafson, Jeffrey L.
, p. 13895 - 13905 (2020/11/03)
We report a highly efficient ortho-selective electrophilic chlorination of phenols utilizing a Lewis basic selenoether catalyst. The selenoether catalyst resulted in comparable selectivities to our previously reported bis-thiourea ortho-selective catalyst, with a catalyst loading as low as 1%. The new catalytic system also allowed us to extend this chemistry to obtain excellent ortho-selectivities for unprotected anilines. The selectivities of this reaction are up to >20:1 ortho/para, while the innate selectivities for phenols and anilines are approximately 1:4 ortho/para. A series of preliminary studies revealed that the substrates require a hydrogen-bonding moiety for selectivity.
Thiazolidine derivatives
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, (2008/06/13)
The invention relates to thiazolidine derivatives having in 4-position a hydroxy group and a 3'-sulphamyl-phenyl substituent, in 2-position an imino group and in 1-position an aliphatic or cycloaliphatic substituent. Said thiazolidines have diuretic activity. The invention also relates to a process for the manufacture of said compounds.
