57319-78-5 Usage
General Description
"(E)-3-(4-(dimethylamino)phenyl)-2-(1-methyl-1H-benzo[d]imidazol-2-yl)acrylonitrile" is a chemical compound with a complex structure consisting of a (E)-configured acrylonitrile group attached to a 2-(1-methyl-1H-benzo[d]imidazol-2-yl) group, which in turn is linked to a 4-(dimethylamino)phenyl group. (E)-3-(4-(dimethylamino)phenyl)-2-(1-methyl-1H-benzo[d]imidazol-2-yl)acrylonitrile has potential applications in the field of organic synthesis, as well as in medicinal chemistry due to its structural features that may confer biological activity. It is important to handle and use this compound with care, following proper safety measures and regulations to avoid potential hazards. Further research and testing may be needed to fully understand and utilize the properties and potential applications of this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 57319-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,3,1 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57319-78:
(7*5)+(6*7)+(5*3)+(4*1)+(3*9)+(2*7)+(1*8)=145
145 % 10 = 5
So 57319-78-5 is a valid CAS Registry Number.
57319-78-5Relevant articles and documents
Unexpected regiospecific reduction of the double bond by NaBH4 in 2-(1-methyl/1H-benzimidazole-2-yl)-3-aryl-acrylonitrile
Dubey,Reddy, P. V. V. Prasada
, p. 2259 - 2266 (2008/02/07)
Condensation of (1H-benzimidazole-2-yl)-acetonitrile 1 with aromatic aldehydes in 5% NaOH solution gave the corresponding 2-(1H-benzimidazole-2-yl)- 3-aryl-acrylonitrile 2, which on treatment with NaBH4 in ethanol unexpectedly gave 2-(1H-benzimidazole-2-yl)-3-aryl-propionitrile 3 by the regiospecific reduction of the double bond. Shaking a solution of 2 with H2/Pd-C in methanol also gave 3. Reaction of 2 with DMS gave the corresponding N-methylated analogue 5, which also with NaBH4 gave 6, once again by the regiospecific reduction of the double bond as in the case of 1-demethylated analogue (i.e., 2). Copyright Taylor & Francis Group, LLC.
