85355-50-6 Usage
Uses
Used in Pharmaceutical Industry:
(2-Bromo-6-nitro-phenyl)-acetaldehyde is used as an intermediate in the synthesis of various biologically active compounds for the development of advanced pharmaceuticals. Its unique structure with both bromine and nitro groups in the phenyl ring allows for the creation of a diverse range of pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Production:
(2-Bromo-6-nitro-phenyl)-acetaldehyde is also used in the production of agrochemicals, where its reactivity and functional groups contribute to the development of effective products for agricultural applications.
Used in Dye Manufacturing:
(2-Bromo-6-nitro-phenyl)-acetaldehyde is utilized in the manufacturing of dyes due to its ability to form a variety of colored compounds, making it a valuable component in the dye industry.
Used in Organic Synthesis:
As a versatile building block, (2-Bromo-6-nitro-phenyl)-acetaldehyde is used in organic synthesis to produce a wide range of important chemical compounds, showcasing its utility across various chemical and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 85355-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85355-50:
(7*8)+(6*5)+(5*3)+(4*5)+(3*5)+(2*5)+(1*0)=146
146 % 10 = 6
So 85355-50-6 is a valid CAS Registry Number.
85355-50-6Relevant academic research and scientific papers
Heterocyclic sulfonamide derivatives
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Page 15, (2010/11/29)
The present invention provides certain heterocyclic sulfonamide derivatives of formula (I): useful for potentiating glutamate receptor function in a patient and therefore, useful for treating a wide variety of conditions, such as psychiatric and neurological disorders.
Synthesis of Substituted Indoles via Meerwein Arylation
Raucher, Stanley,Koolpe, Gary A.
, p. 2066 - 2069 (2007/10/02)
A new method for the synthesis of substituted indoles is detailed.Meerwein arylation of 4- and 6-substituted 2-nitrobenzenediazonium chlorides with vinyl acetate or vinyl bromide and subsequent reductive cyclization of the resulting adducts affords the corresponding 6- and 4-substituted (CH3, OCH3, Cl, Br, CF3) indoles.The diazonium bisulfates of weakly basic 2-nitroanilines (4-Cl, 6-Br, 4-CF3) gave higher yields of Meerwein arylation adducts than the corresponding diazonium chlorides.Coupling of 2-nitrobenzenediazonium chloride with 2-acetoxy-1-alkenes followed byreductive cyclization affords 2-alkylindoles.
