14371-17-6 Usage
Description
(2E)-2-(3,4-dimethoxybenzylidene)-1,1-dimethylhydrazine, also known as DMH, is a chemical compound belonging to the hydrazine family with the molecular formula C12H18N2O2. It is characterized as a yellowish liquid with a strong, pungent odor and is flammable. As a hazardous chemical, DMH is toxic and requires careful handling to avoid potential health hazards.
Uses
Used in Pharmaceutical and Agrochemical Industries:
DMH is utilized as an intermediate in the synthesis of various pharmaceutical and agrochemical products, contributing to the development of new drugs and pesticides.
Used in Organic Synthesis:
In addition to its applications in pharmaceuticals and agrochemicals, DMH also serves as a precursor in organic synthesis, enabling the creation of a range of chemical compounds for different purposes.
Used in Pesticide Preparation:
DMH is primarily employed as a precursor in the preparation of pesticides, playing a crucial role in the development of effective and targeted pest control solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 14371-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,7 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14371-17:
(7*1)+(6*4)+(5*3)+(4*7)+(3*1)+(2*1)+(1*7)=86
86 % 10 = 6
So 14371-17-6 is a valid CAS Registry Number.
14371-17-6Relevant articles and documents
Hydrazone as the directing group for Ir-catalyzed arene diborylations and sequential functionalizations
Ros, Abel,Lopez-Rodriguez, Rocio,Estepa, Beatriz,Alvarez, Eleuterio,Fernandez, Rosario,Lassaletta, Jose M.
supporting information; experimental part, p. 4573 - 4576 (2012/04/23)
The use of hemilabile pyridine-hydrazone N,N-ligands allows the highly selective Ir-catalyzed ortho,ortho'-directed diborylation of aromatic N,N-dimethylhydrazones in near-quantitative yields. One-pot sequential Suzuki-Miyaura cross-coupling with different aryl bromides provides a short entry to unsymmetrically substituted 2,6-diarylbenzaldehyde derivatives.
