56475-44-6 Usage
Uses
Used in Organic Synthesis:
5-iodo-2,2-dimethylpentanenitrile is used as a reactive intermediate for the synthesis of various nitrogen-containing compounds, leveraging its reactivity to form new chemical entities with potential applications in different industries.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 5-iodo-2,2-dimethylpentanenitrile is used as a precursor in the production of drugs, contributing to the development of new medications with diverse therapeutic profiles.
Used in Agrochemical Production:
5-iodo-2,2-dimethylpentanenitrile also finds application in the agrochemical sector, where it is employed as a starting material for the synthesis of pesticides and other crop protection agents, enhancing agricultural productivity and crop protection.
Given the compound's flammable and corrosive nature, it is imperative that safety precautions are strictly adhered to during its use in any application, ensuring the well-being of personnel and the integrity of the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 56475-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56475-44:
(7*5)+(6*6)+(5*4)+(4*7)+(3*5)+(2*4)+(1*4)=146
146 % 10 = 6
So 56475-44-6 is a valid CAS Registry Number.
56475-44-6Relevant academic research and scientific papers
SEMICONDUCTING COMPOSITIONS COMPRISING SEMICONDUCTING POLYMERS
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Paragraph 0583-0585, (2019/05/15)
A semiconducting composition comprising a semiconducting polymer and a semiconducting non-polymeric polycyclic compound, wherein the semiconducting polymer comprises units of A and/or B: wherein R1, R2, R5, R6, R7, R8, x, y, p, q, r, R3, R4, R9, R10 and R11 have any of the meanings defined in the description.
Catalytic asymmetric synthesis of a tertiary benzylic carbon center via phenol-directed alkene hydrogenation
Caille, Seb,Crockett, Rich,Ranganathan, Krishnakumar,Wang, Xiang,Woo, Jacqueline C. S.,Walker, Shawn D.
experimental part, p. 5198 - 5206 (2011/08/09)
An expeditious synthetic approach to chiral phenol 1, a key building block in the preparation of a series of drug candidates, is reported. The strategy includes a cost-effective and readily scalable route to cyclopentanone 3 from isobutyronitrile (10). The sterically hindered and enolizable ketone 3 was subsequently employed in a challenging Grignard addition mediated by LaCl 3?2LiCl. A novel preparation of the lanthanide reagent required for this transformation is described. To complete the process, a highly enantioselective hydrogenation step afforded the target (1). The importance of the phenol group to the success of this asymmetric transformation is discussed.
