56071-99-9 Usage
Uses
Used in Agriculture:
(3,4-dichlorophenyl)(hydroxy)acetic acid is used as a herbicide for controlling the growth of unwanted plants, such as weeds, in various types of crops. It helps in disrupting the growth and development processes of these plants, thereby promoting healthier crop growth.
Used in Aquatic Weed Control:
(3,4-dichlorophenyl)(hydroxy)acetic acid is used as a plant growth regulator for controlling aquatic weeds. It is effective in managing the growth of unwanted plants in water bodies, thus maintaining a clean and healthy aquatic environment.
Used in Environmental Remediation:
(3,4-dichlorophenyl)(hydroxy)acetic acid has been studied for its potential use in environmental remediation. Its ability to disrupt the growth and development of plants can be utilized in the management of invasive plant species and the restoration of natural habitats.
Used in Synthesis of Biologically Active Compounds:
(3,4-dichlorophenyl)(hydroxy)acetic acid serves as a building block for the synthesis of other biologically active compounds. Its unique chemical structure allows it to be a valuable component in the development of new pharmaceuticals and other bioactive substances.
Check Digit Verification of cas no
The CAS Registry Mumber 56071-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,7 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56071-99:
(7*5)+(6*6)+(5*0)+(4*7)+(3*1)+(2*9)+(1*9)=129
129 % 10 = 9
So 56071-99-9 is a valid CAS Registry Number.
56071-99-9Relevant academic research and scientific papers
Enantioselective C-H Olefination of α-Hydroxy and α-Amino Phenylacetic Acids by Kinetic Resolution
Xiao, Kai-Jiong,Chu, Ling,Yu, Jin-Quan
supporting information, p. 2856 - 2860 (2016/02/27)
Significant progress has been made in the past decade regarding the development of enantioselective C-H activation reactions by desymmetrization. However, the requirement for the presence of two chemically identical prochiral C-H bonds represents an inherent limitation in scope. Reported is the first example of kinetic resolution by a palladium(II)-catalyzed enantioselective C-H activation and C-C bond formation, thus significantly expanding the scope of enantioselective C-H activation reactions.
Synthesis of dichlorophenyl-, cyanophenyl-and quinolinyl-substituted α-ethoxyacetic acids and derivatives, via α-hydroxyarylacetic acids
Gutteridge, Clare E.,Curtis, Sean M.,Major, Joshua W.,Nin, Daniel A.,Bhattacharjee, Apurba K.,Nichols, Daniel A.,Gerena, Lucia
, p. 407 - 412 (2016/03/25)
A synthetic approach to novel series of α-ethoxy-α-phenylacetamides and α-ethoxy-α-quinolinylacetamides was developed. Aryl aldehydes were converted to cyanohydrins, which were then hydrolyzed or alcoholyzed. Following ethylation of the α-hydroxy group, p
