38629-93-5 Usage
Compound type
Organic compound
Structure
Substituted aniline derivative with a phenylamine functional group attached to a 2',6'-dimethylphenoxy group
Usage
Raw material in the synthesis of various pharmaceuticals, dyes, and other organic compounds
Physical state
Stable and colorless solid at room temperature
Handling and storage
Typically handled and stored under standard laboratory conditions
Uses and applications
Vary depending on the specific synthesis or reaction it is being used for
Check Digit Verification of cas no
The CAS Registry Mumber 38629-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,2 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38629-93:
(7*3)+(6*8)+(5*6)+(4*2)+(3*9)+(2*9)+(1*3)=155
155 % 10 = 5
So 38629-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO/c1-10-6-5-7-11(2)14(10)16-13-9-4-3-8-12(13)15/h3-9H,15H2,1-2H3
38629-93-5Relevant academic research and scientific papers
The neuronal calcium ion channel activity of constrained analogues of MONIRO-1
Bispat, Anjie,Cardoso, Fernanda C.,Duggan, Peter J.,Geoffroy, Chloe,Lewis, Richard J.,Marliac, Marie-Adeline,Schmit, Matthieu,Tuck, Kellie L.
, (2020/07/28)
Structural modifications of the neuronal calcium channel blocker MONIRO-1, including constraining the phenoxyaniline portion of the molecule and replacing the guanidinium functionality with tertiary amines, led to compounds with significantly improved aff
