41470-05-7 Usage
Uses
Used in Vision Restoration and Reconstitution Treatments:
11-cis-3,4-Didehydro Retinal is used as a key component in vision restoration and reconstitution treatments. It is particularly important for individuals suffering from certain retinal diseases or conditions that affect the function of the retina, such as retinitis pigmentosa or age-related macular degeneration. The application of 11-cis-3,4-Didehydro Retinal helps in restoring the light-sensitive function of the retina, thereby improving vision and overall quality of life for affected individuals.
In the field of ophthalmology, 11-cis-3,4-Didehydro Retinal is used as a therapeutic agent for treating various vision-related disorders. Its application in this industry is based on its ability to enhance the light-sensitive properties of the retina, which is essential for maintaining normal vision.
Additionally, 11-cis-3,4-Didehydro Retinal is also used in research and development for creating new treatments and therapies related to vision restoration. Its unique properties make it a valuable tool for scientists and researchers working on innovative solutions to combat vision loss and improve the lives of those affected by vision-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 41470-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,7 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41470-05:
(7*4)+(6*1)+(5*4)+(4*7)+(3*0)+(2*0)+(1*5)=87
87 % 10 = 7
So 41470-05-7 is a valid CAS Registry Number.
41470-05-7Relevant academic research and scientific papers
A convenient and stereoselective synthesis of 11Z-3,4-didehydroretinal by Horner-Emmons reaction using diphenyl phosphonate
Wada, Akimori,Wang, Fei,Ito, Masayoshi
, p. 112 - 114 (2008/09/18)
A convenient synthesis of 3,4-didehydroretinal was developed. The Horner-Emmons reaction between 3,4-didehydro-β-ionone and diphenyl phosphonate in the presence of crown ether gave the retinonitrile as an isomeric mixture, in which the newly produced double bond was predominantly 11Z-form. After separation of the 11Z-form retinonitrile, it was converted into the corresponding retinal in good yield without isomerization of the double bonds.
