265652-39-9 Usage
General Description
4-Bromo-3-methylthiophenecarboxylic acid is a chemical compound with a scientific formula of C6H5BrO2S. It is commonly used in the synthesis of other chemical compounds, and is valuable in the field of organic chemistry due to its bromine and carboxylic acid functional groups; these enable it to participate in a variety of reactions. It is characterized by its phenyl ring structure with a single bromine atom substitution, a methylthio group, and a carboxylic acid functional group. The properties of this chemical compound, such as reactivity and stability, largely depend on these functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 265652-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,6,5 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 265652-39:
(8*2)+(7*6)+(6*5)+(5*6)+(4*5)+(3*2)+(2*3)+(1*9)=159
159 % 10 = 9
So 265652-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrO2S/c1-3-4(7)2-10-5(3)6(8)9/h2H,1H3,(H,8,9)
265652-39-9Relevant articles and documents
FUSED THIOPHENE COMPOUNDS
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Paragraph 0142, (2020/01/08)
The present disclosure provides compounds that modulate protein function of 1 L-1β, IL-2, IL-6, TNF-α, CK1α, GSPT1, aiolos, ikaros or helios, to restore protein homeostasis, and 1 cell-cell adhesion. The disclosure provides methods of modulating protein-mediated diseases, such as cytokine-mediated diseases, disorders, conditions, or responses. Compositions, including in combination with other cytokine and inflammatory mediators are provided. Uses of compounds for treatment or amelioration of diseases, disorders, or conditions associated with a protein, are also provided.
Process for preparing 3-(substituted phenyl)-5-thienyl or furyl)-1,2,4-triazoles and novel intermediates utilized therein
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, (2008/06/13)
New synthetic procedures for preparing insecticidal 3-(substituted phenyl)-5-(thienyl or furyl)-1,2,4-triazoles utilizing thioimidate intermediate.
