648412-53-7 Usage
General Description
4,5-Dibromo-3-methyl-thiophene-2-carboxylic acid methyl ester is a chemical compound with the molecular formula C8H7Br2O2S. It is a methyl ester derivative of 4,5-dibromo-3-methylthiophene-2-carboxylic acid, which is commonly used in organic synthesis and pharmaceutical research. This chemical is a yellowish to brown solid with a molecular weight of 311.007 g/mol. It is known for its use as an intermediate in the production of various pharmaceuticals and agrochemicals, as well as in the field of material science for the development of new materials and compounds. However, its specific uses and properties may vary depending on the application and research field.
Check Digit Verification of cas no
The CAS Registry Mumber 648412-53-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,4,1 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 648412-53:
(8*6)+(7*4)+(6*8)+(5*4)+(4*1)+(3*2)+(2*5)+(1*3)=167
167 % 10 = 7
So 648412-53-7 is a valid CAS Registry Number.
648412-53-7Relevant articles and documents
Synthesis and pharmacological characterization of N3-substituted willardiine derivatives: Role of the substituent at the 5-position of the uracil ring in the development of highly potent and selective GLUK5 kainate receptor antagonis
Dolman, Nigel P.,More, Julia C. A.,Alt, Andrew,Knauss, Jody L.,Pentik?inen, Olli T.,Glasser, Carla R.,Bleakman, David,Mayer, Mark L.,Collingridge, Graham L.,Jane, David E.
, p. 1558 - 1570 (2007/10/03)
Some N3-substituted analogues of willardiine such as 11 and 13 are selective kainate receptor antagonists. In an attempt to improve the potency and selectivity for kainate receptors, a range of analogues of 11 and 13 were synthesized with 5-sub
Novel thienopyridine compounds, and methods of use thereof
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Page/Page column 35, (2008/06/13)
The present invention relates to novel compounds capable of modulating the stability and/or activity of hypoxia inducible factor (HIF).
