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37984-23-9

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37984-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37984-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,8 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37984-23:
(7*3)+(6*7)+(5*9)+(4*8)+(3*4)+(2*2)+(1*3)=159
159 % 10 = 9
So 37984-23-9 is a valid CAS Registry Number.

37984-23-9Downstream Products

37984-23-9Relevant academic research and scientific papers

A rapid and specific derivatization procedure to identify acyl-glucuronides by mass spectrometry

Vaz, Alfin D. N.,Wang, Wei Wei,Bessire, Andrew J.,Sharma, Raman,Hagen, Anne E.

, p. 2109 - 2121 (2010)

A simple procedure is described to identify acyl-glucuronides by coupled liquid chromatography/ mass spectrometry after derivatization to a hydroxamic acid with hydroxylamine. The reaction specificity obviates the need for isolation of the acyl-glucuronid

Polyfunctional action of biologically active compounds in antitumor chemotherapy of cyclophosphamide

Bogatyrenko,Konovalova,Sipyagin,Bogatyrenko,Kuropteva,Baider,Sashenkova,Fedorov

, (2014)

Combinations of the known cytostatic cyclophosphamide (cyclophosphan) with hydroxamic acids (asparagylhydroxamic and salicylhydroxamic), nitric oxide donor (sodium nitrate), and an original hybrid non-steroidal anti-inflammatory compound, viz., diclofenac

Antiphlogistic phenylacetohydroxamic acid compositions

-

, (2008/06/13)

Phenylacetohydroxamic acids having the formula I STR1 wherein R1, R2, R3 and R4, independently of each other, represent hydrogen, chlorine, fluorine or bromine atoms or an alkyl or alkoxy group having at most 6 carbon atoms, and wherein R2 may additionally represent a trifluoromethyl group with the proviso that R1, R2 and R3 may not simultaneously represent hydrogen atoms and their pharmaceutically acceptable salts with bases, which compounds inhibit plateletaggregation and exhibit valuable pharmacological, in particular, antiphlogistic, analgesic and antipyretic activity.

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