93794-06-0 Usage
General Description
3-(1-(2-benzoxazolyl)hydrazino)propanenitrile is a chemical compound consisting of a hydrazine functional group attached to a propanenitrile moiety with a benzoxazole ring. It is commonly used as a reagent in organic synthesis reactions due to its ability to form stable hydrazones, which can be further functionalized to form various organic compounds. The benzoxazole ring also imparts fluorescence properties to the compound, making it useful in the development of fluorescent probes and sensors for biological applications. Additionally, the nitrile group in the molecule can undergo various chemical reactions to produce a wide range of derivatives for potential pharmaceutical or material science applications.
Check Digit Verification of cas no
The CAS Registry Mumber 93794-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,9 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93794-06:
(7*9)+(6*3)+(5*7)+(4*9)+(3*4)+(2*0)+(1*6)=170
170 % 10 = 0
So 93794-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N4O/c11-6-3-7-14(12)10-13-8-4-1-2-5-9(8)15-10/h1-2,4-5H,3,7,12H2
93794-06-0Relevant articles and documents
3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: Inhibitors of immune complex induced inflammation
Haviv,Ratajczyk,DeNet,Kerdesky,Walters,Schmidt,Holms,Young,Carter
, p. 1719 - 1728 (2007/10/02)
3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives were evaluated in the dermal and pleural reverse passive Arthus reactions in the rat. In the pleural test these compounds were effective in reducing exudate volume and accumulation of white blood cells. This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin. The structural requirements for inhibiting the Arthus reactions were studied by systematic chemical modification of 1. These structure-activity relationship studies revealed that nitrogen 1' of the hydrazino group is essential for activity and must be electron rich, whereas chemical modifications of other sites of 1 had only a modest effect on activity.
