104670-71-5 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 3-bromo-2-nitrobenzoate is used as an intermediate in the synthesis of pharmaceuticals. Its presence in the compound allows for various chemical reactions and transformations, contributing to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 3-bromo-2-nitrobenzoate is utilized as a building block for the creation of agrochemicals. Its unique functional groups enable the synthesis of compounds that can be used in the development of pesticides and other agricultural chemicals.
Used in Dye Industry:
Methyl 3-bromo-2-nitrobenzoate is also used in the dye industry as an intermediate for the production of dyes. Its chemical properties allow for the creation of a wide range of colored compounds, making it a valuable component in the synthesis of various dyes.
Used in Organic Synthesis:
As a versatile chemical compound, Methyl 3-bromo-2-nitrobenzoate is used in organic synthesis for the preparation of various complex chemical compounds. Its nitro and bromo functional groups make it a potential candidate for numerous chemical reactions, facilitating the synthesis of a broad range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 104670-71-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,7 and 0 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104670-71:
(8*1)+(7*0)+(6*4)+(5*6)+(4*7)+(3*0)+(2*7)+(1*1)=105
105 % 10 = 5
So 104670-71-5 is a valid CAS Registry Number.
104670-71-5Relevant academic research and scientific papers
Lindner, Stephanie,Nieger, Martin,Br?se, Stefan
, p. 3303 - 3308 (2015)
Herein, the synthesis of heteromeric tetrahydroxanthone biaryls is described, a widespread core structure of many natural products. The development of both stannylation and Stille coupling procedures of base-sensitive tetrahydroxanthones enabled their cou
Synthesis of hexacyclic parnafungin A and C models
Zhou, Quan,Snider, Barry B.
experimental part, p. 8224 - 8233 (2011/02/23)
A convergent, practical route to unstable hexacyclic parnafungin A and C models has been developed. Two iodoxanthones were prepared in four or five steps (33-50% overall yield). Suzuki-Miyaura coupling of the iodoxanthones with excess readily available 3-
Tunable emissive thin films through ICT photodisruption of nitro-substituted triarylamines
Jacquart, Aurelie,Tauc, Patrick,Pansu, Robert B.,Ishow, Elena
experimental part, p. 4360 - 4362 (2010/08/22)
UV-assisted photocleavage in the solid state of orange emitting nitro-substituted triarylamines leads to the appearance of blue emission following photodisruption of the ICT state.
