701-34-8 Usage
Description
4-Bromobenzenesulfonamide is a chemical compound that serves as a metabolite of ebrotidine, a novel H2-receptor antagonist. It is characterized by its unique chemical structure and properties, making it a versatile compound for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
4-Bromobenzenesulfonamide is used as a reagent for the preparation of cobalt(III) complexes of N,R-sulfonyldithiocarbimate anion. It plays a crucial role in the synthesis process, contributing to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-Bromobenzenesulfonamide is utilized in the synthesis of 2-, 3-, and 4-(substituted-phenylethynyl)benzenesulfonamides. These synthesized compounds can be further used in the development of various chemical products, including pharmaceuticals, dyes, and other specialty chemicals.
Overall, 4-Bromobenzenesulfonamide is a valuable compound with applications in the pharmaceutical and chemical synthesis industries, contributing to the development of new compounds and products with potential benefits in various sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 701-34-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 701-34:
(5*7)+(4*0)+(3*1)+(2*3)+(1*4)=48
48 % 10 = 8
So 701-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H6BrNO2S/c7-5-2-1-3-6(4-5)11(8,9)10/h1-4H,(H2,8,9,10)
701-34-8Relevant articles and documents
METHOD FOR PRODUCING OXIDE USING BETA-MANGANESE DIOXIDE
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Paragraph 0097; 0098, (2021/10/15)
With the object of efficiently producing an oxidation product, the present invention provides a method for producing an oxidation product by oxidizing a raw material compound in the presence of oxygen, wherein the raw material compound is oxidized in the presence of manganese dioxide having a crystal structure of β-type.
Unlocking Amides through Selective C–N Bond Cleavage: Allyl Bromide-Mediated Divergent Synthesis of Nitrogen-Containing Functional Groups
Govindan, Karthick,Chen, Nian-Qi,Chuang, Yu-Wei,Lin, Wei-Yu
, p. 9419 - 9424 (2021/11/30)
We report a new set of reactions based on the unlocking of amides through simple treatment with allyl bromide, creating a common platform for accessing a diverse range of nitrogen-containing functional groups such as primary amides, sulfonamides, primary amines, N-acyl compounds (esters, thioesters, amides), and N-sulfonyl esters. The method has potential industrial applicability, as demonstrated through gram-scale syntheses in batch and in a continuous flow system.
NAPHTHYRIDINE DERIVATIVES AS PRC2 INHIBITORS
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Paragraph 0371-0372, (2020/11/03)
Disclosed are compounds of formula (I) or (II) that inhibit Polycomb Repressive Complex 2 (PRC2) activity. In particular, the present invention relates to compounds, pharmaceutical compositions and methods of use, such as methods of treating cancer using the compounds and pharmaceutical compositions of the present invention.