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2-(2-phenyl-1,3-benzoxazol-6-yl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51234-94-7

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51234-94-7 Usage

Antioxidant properties

It helps neutralize harmful free radicals, potentially benefiting skincare and cosmetic products.

Anti-inflammatory properties

Coumarin may help reduce inflammation, making it a potential ingredient in skincare products.

Check Digit Verification of cas no

The CAS Registry Mumber 51234-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,3 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51234-94:
(7*5)+(6*1)+(5*2)+(4*3)+(3*4)+(2*9)+(1*4)=97
97 % 10 = 7
So 51234-94-7 is a valid CAS Registry Number.

51234-94-7Downstream Products

51234-94-7Relevant academic research and scientific papers

IMIDAZOLE DERIVATIVES AS IDO INHIBITORS

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Page/Page column 136, (2011/06/11)

Presently provided are IDO inhibitors of general formulae (VII), (VIII) as shown below and pharmaceutical compositions thereof, useful for modulating an activity of indoleamine 2,3-dioxygenase; treating indoleamine 2,3-dioxygenase (IDO) mediated immunosuppression; treating a medical conditions that benefit from the inhibition of enzymatic activity of indoleamine-2,3-dioxygenase; enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent; treating tumor-specific immunosuppression associated with cancer; and treating immunosupression associated with an infectious disease.

Benzoxazole derivatives in treating inflammation, pain and fever

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, (2008/06/13)

The invention provides novel 5- and 6-benzoxazolyl alkanoic acids, optionally substituted in the 2-position, and derivatives thereof which possess anti-inflammatory, anti-pyretic and analgesic activity. Also provided is a process for preparing such compounds by cyclising an appropriately substituted o-aminophenol and, if necessary, converting the resultant benzoxazole to the desired compound.

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