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5-Benzoxazolecarboxaldehyde, 2,3-dihydro-2-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

581102-27-4

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581102-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 581102-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,1,1,0 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 581102-27:
(8*5)+(7*8)+(6*1)+(5*1)+(4*0)+(3*2)+(2*2)+(1*7)=124
124 % 10 = 4
So 581102-27-4 is a valid CAS Registry Number.

581102-27-4Downstream Products

581102-27-4Relevant academic research and scientific papers

CHROMEN-4-ONE DERIVATIVES, SUCH AS E.G. FLAVONES, FOR USE AS CK2 INHIBITORS FOR THE TREATMENT OF NEUROINFLAMMATION

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Sheet 39, (2021/11/26)

Chromen-4-one derivatives, such as e.g. flavone derivatives and pharmaceutical compositions thereof are disclosed. In some instances, the compounds have increased aqueous solubility, bioavailability, and ability to cross the blood-brain-barrier. The compounds may be used to inhibit casein kinase 2 (CK2) activity and/or to treat diseases and conditions mediated at least in part by CK2 enzyme, such as e.g. inflammation, in particular neuroinflammation, or other diseases, such as e.g. cancer, cardiac hypertrophy, cystic fibrosis, a neurodegenerative disease, bipolar disorder, depression, a viral infection, obesity, diabetes mellitus, atherosclerosis, epilepsy, or any combination thereof.

NEW CYCLOHEXYL AND QUINUCLIDINYL CARBAMATE DERIVATIVES HAVING BETA2 ADRENERGIC AGONIST AND M3 MUSCARINIC ANTAGONIST ACTIVITY

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Page/Page column 41; 42; 94, (2014/07/08)

The present invention relates to novel compounds having β2 adrenergic agonist and M3 muscarinic antagonist dual activity, to pharmaceutical compositions containing them, to the process for their preparation and to their use in respiratory therapies.

5-Quinoline derivatives having an anti-bacterial activity

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Page/Page column 17, (2010/12/31)

The present invention describes novel anti-bacterial compounds of the formula (I). These compounds are, amongst others, of interest as inhibitors of DNA gyrase and topoisomerases, for example of topoisomerase II and IV.

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