59346-56-4 Usage
Molecular weight
141.21 g/mol
Type of compound
Aliphatic nitrile
Structural features
Hydroxyl group, branched carbon chain
Usage
Synthesis of pharmaceuticals, agrochemicals, flavors, and fragrances
Primary use
Intermediate in manufacturing of products such as insecticides, herbicides, and pharmaceuticals
Additional use
Building block for synthesis of various organic compounds
Check Digit Verification of cas no
The CAS Registry Mumber 59346-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,4 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59346-56:
(7*5)+(6*9)+(5*3)+(4*4)+(3*6)+(2*5)+(1*6)=154
154 % 10 = 4
So 59346-56-4 is a valid CAS Registry Number.
59346-56-4Relevant articles and documents
One-pot oxidative conversion of alcohols into nitriles by using a TEMPO/PhI(OAc)2/NH4OAc system
Vatèle, Jean-Michel
, p. 1275 - 1278 (2014/06/10)
A direct conversion of alcohols into nitriles with 2,2,6,6- tetramethylpiperidine-1-oxyl (TEMPO), iodosobenzene diacetate, and ammonium acetate as a nitrogen source is reported. This transformation, which proceeds through an oxidation-imination-aldimine oxidation sequence in situ, has been applied to a range of aliphatic, benzylic, heteroaromatic, allylic, and propargyl alcohols. Highly chemoselective ammoxidation of primary alcohols in the presence of secondary alcohols was also achieved. Georg Thieme Verlag Stuttgart New York.
