3408-30-8 Usage
Synonyms
Dihydronaphthoic acid
Appearance
White crystalline solid
Solubility
Soluble in organic solvents, insoluble in water
Chemical structure
Unique chemical structure that allows for versatile synthesis
Pharmaceutical synthesis
Used as an intermediate in the production of various pharmaceuticals
Antiviral drugs
Utilized in the synthesis of antiviral drugs
Natural products
Acts as a building block in the synthesis of natural products
Corrosion inhibition
Potential application as a corrosion inhibitor
Polymer chemistry
Has potential applications in polymer chemistry
Check Digit Verification of cas no
The CAS Registry Mumber 3408-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,0 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3408-30:
(6*3)+(5*4)+(4*0)+(3*8)+(2*3)+(1*0)=68
68 % 10 = 8
So 3408-30-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2/c12-11(13)10-6-5-8-3-1-2-4-9(8)7-10/h1-6,10H,7H2,(H,12,13)
3408-30-8Relevant academic research and scientific papers
A new, potent, conformationally restricted analogue of amphetamine: 2-Amino-1,2-dihydronapthalene
Hathaway,Nichols,Nichols,Yim
, p. 535 - 538 (2007/10/02)
A new stimulant compound, 1,2-dihydro-2-naphthalenamine (2-amino-1,2-dihydronaphthalene, 2-ADN), was prepared as an analogue of amphetamine and of 2-aminotetralin. The optical isomers of 2-ADN were obtained by chemical resolution, and the absolute configuration was determined to be R-(+) and S-(-). Preliminary pharmacological evaluation revealed that racemic 2-ADN is approximately one-fourth as potent as (+)-amphetamine as a stimulant in mice. The S-(-) isomer of 2-ADN was found to be solely responsible for the stimulant effects of the racemate. Both reserpine and α-methyl-p-tyrosine antagonized the stimulation produced by 2-ADN.
