13608-36-1 Usage
Description
(1E)-1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine is a hydrazone compound with the molecular formula C12H16N4O4. It is a yellow crystalline solid that is commonly used in organic synthesis and as a building block for the production of other chemical compounds. Its structure contains a dinitrophenyl group, which is a common functional group in organic chemistry that is often used as a protecting group or a precursor in the synthesis of various compounds. This versatile and valuable chemical building block has potential applications in pharmaceuticals, agrochemicals, and materials science.
Uses
Used in Organic Synthesis:
(1E)-1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a building block in organic synthesis for the production of other chemical compounds. Its unique structure and properties make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
(1E)-1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a chemical intermediate in the pharmaceutical industry for the development of new drugs. Its structure and properties can be utilized to create novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
(1E)-1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a starting material in the agrochemical industry for the synthesis of various agrochemicals. Its potential applications in this field include the development of new pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science:
(1E)-1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine is used as a component in the development of new materials in materials science. Its unique structure and properties can contribute to the creation of innovative materials with various applications, such as in coatings, adhesives, or other industrial materials.
Check Digit Verification of cas no
The CAS Registry Mumber 13608-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,0 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13608-36:
(7*1)+(6*3)+(5*6)+(4*0)+(3*8)+(2*3)+(1*6)=91
91 % 10 = 1
So 13608-36-1 is a valid CAS Registry Number.
13608-36-1Relevant articles and documents
Selective reduction of carboxylic acids to aldehydes catalyzed by B(C 6F5)3
Bezier, David,Park, Sehoon,Brookhart, Maurice
, p. 496 - 499 (2013/03/29)
B(C6F5)3 efficiently catalyzes hydrosilylation of aliphatic and aromatic carboxylic acids to produce disilyl acetals under mild conditions. Catalyst loadings can be as low as 0.05 mol %, and bulky tertiary silanes are favored to give selectively the acetals. Acidic workup of the disilyl acetals results in the formation of aldehydes in good to excellent yields.
Kinetics and mechanism of the oxidation of aliphatic primary alcohols by imidazolium fluorochromate
Gehlot,Gilla,Mishra,Sharma, Vinita
experimental part, p. 685 - 692 (2012/04/04)
The oxidation of nine aliphatic primary alcohols by imidazolium fluorochromate (IFC) in dimethylsulphoxide leads to the formation of corresponding aldehydes. The reaction is first order with respect to IFC. A Michaelis-Menten type kinetics is observed with respect to alcohols. The reaction is promoted by hydrogen ions; the hydrogen-ion dependence has the form : kobs = a + b [H+]. The oxidation of [1,1- 2H2]ethanol (MeCD2OH) exhibits a substantial primary kinetic isotope effect (kH/kD = 5.87 at 298 K). The reaction has been studied in nineteen different organic solvents. The solvent effect was analysed using Taft's and Swain's multiparametric equations. The rate of oxidation is susceptible to both polar and steric effects of the substituents. A suitable mechanism has been proposed.
Oxidation of unactivated primary aliphatic amines catalyzed by an electrogenerated 3,4-azaquinone species: A small-molecule mimic of amine oxidases
Largeron, Martine,Neudorffer, Anne,Fleury, Maurice-Bernard
, p. 1026 - 1029 (2007/10/03)
High catalytic performance of the electrogenerated amine oxidase mimic 3,4-iminoquinone 1ox is observed under metal-free conditions in the chemoselective oxidation reaction of unactivated primary aliphatic amines.
