1329489-84-0 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-(4'-chloro-[1,1'-biphenyl]-2-yl)acetate is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with specific therapeutic properties. Its unique structure allows it to be a key component in the creation of molecules with targeted biological activities.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 2-(4'-chloro-[1,1'-biphenyl]-2-yl)acetate is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its chemical properties enable it to be incorporated into compounds that can effectively control, repel, or kill pests and weeds, thus protecting crops.
Used in Fragrance Industry:
Methyl 2-(4'-chloro-[1,1'-biphenyl]-2-yl)acetate is also used as a component in the fragrance industry, where it contributes to the creation of complex and unique scents. Its aromatic properties make it a valuable ingredient in the formulation of perfumes, colognes, and other scented products.
Safety Considerations:
It is crucial to handle Methyl 2-(4'-chloro-[1,1'-biphenyl]-2-yl)acetate with care due to its potential harmful effects. Exposure to high levels of Methyl 2-(4'-chloro-[1,1'-biphenyl]-2-yl)acetate can result in skin, eye, and respiratory irritation. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 1329489-84-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,9,4,8 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1329489-84:
(9*1)+(8*3)+(7*2)+(6*9)+(5*4)+(4*8)+(3*9)+(2*8)+(1*4)=200
200 % 10 = 0
So 1329489-84-0 is a valid CAS Registry Number.
1329489-84-0Relevant academic research and scientific papers
Intramolecular aromatic carbenoid insertion of biaryldiazoacetates for the regioselective synthesis of fluorenes
Kim, Jinho,Ohk, Youhwa,Park, Sae Hume,Jung, Yousung,Chang, Sukbok
supporting information; experimental part, p. 2040 - 2047 (2011/10/31)
The rhodium- or copper-catalyzed intramolecular aromatic carbenoid insertion of biaryldiazoacetates offers a convenient route to fluorene carboxylates with high yields. Whereas, thermal conditions provided a mixture of two regioisomeric products when substituted biaryldiazoacetates were employed as substrates. The developed catalytic conditions displayed an excellent level of regioselectivity, presumably owing to steric effects. The insertion mechanism was assumed to be an electrophilic aromatic substitution, which was supported by preliminary mechanistic studies. A chloro-substituted fluorene derivative was efficiently synthesized and utilized as a base-sensitive protecting group of amines.
