112402-18-3 Usage
Type of compound
Psychoactive designer drug
Similarity
Similar in structure and effects to alpha-pyrrolidinopropiophenone (alpha-PPP)
Classification
Synthetic cathinone
Mechanism of action
Acts as a releasing agent of serotonin, norepinephrine, and dopamine
Effects
Stimulant and empathogenic effects
Potential risks
Potential for abuse and harmful side effects
Availability
Often sold as a research chemical or "legal high" alternative to illegal stimulants
Legal status
Regulated or prohibited in many jurisdictions due to potential for harm.
Check Digit Verification of cas no
The CAS Registry Mumber 112402-18-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112402-18:
(8*1)+(7*1)+(6*2)+(5*4)+(4*0)+(3*2)+(2*1)+(1*8)=63
63 % 10 = 3
So 112402-18-3 is a valid CAS Registry Number.
112402-18-3Relevant articles and documents
Synthetic studies of indoles and related compounds. XXVII. A new synthesis of crenatine from ethyl indole-2-carboxylate
Murakami,Yokoyama,Aoki,Suzuki,Sakurai,Shinohara,Miyagi,Kimura,Takahashi,Watanabe,Ohmoto
, p. 2189 - 2195 (1991)
Crenatine (1a), which is a member of a new class of β-carboline alkaloids having an oxygen functionality at the 4-position, was synthesized starting from ethyl 1-benzylindole-2-carboxylate (12a) via cyclization of an elaborated C2-substituent to the 3-position of the indole nucleus and aluminum chloride-catalyzed debenzylation of the protected indolic nitrogen. 1-Ethyl-4-hydroxy-9-methyl-β-carboline (26b), a positional isomer of crenatine with regard to the methyl group, was also synthesized through the same methodology.
