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| Appearance: | Crystals | Color: | Not Pure White |
|---|---|---|---|
| Appliaction: | Research | Chemicals Name: | 4-EFMC |
| CAS: | 843221-23-2 | Purity: | 99.7%min |
| High Light: | research chemicals mephedrone,4mmc crystal |
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High Purity 4-EFMC 4 MMC Research Chemicals Crystal CAS 843221-23-2
| CAS: |
843221-23-2
|
| Formula: |
C11H14FNO
|
| Molecular weight: |
195.233
|
| Compound purity: |
> 99.7%
|
| Appearance: |
Crystals
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| IUPAC: |
2-amino-1-[4-(2-fluoroethyl)phenyl]propan-1-one
|
| Synonyms: |
4-EFC
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4-EFMC with an IUPAC name of 2-amino-1-[4-(2-fluoroethyl)phenyl]propan-1-one and a molecular weight of 195.2334 is a new research compound. The chemical formula is C11H14FNO. Since the chemical is new on the market, there is no research available at this time.
Research on compound was conducted by ACD/Labs’ and ChemAxon. Properties that were predicted by ACD/Labs showed 2 #H bond acceptors, 1 #H bond donor, 3 #Freely rotating bonds, index of refraction at 1.529 with a surface tension of 37.459 dyne/cm, a flash point of 136.924 °C and a boiling point of 302.791 °C at 760 mmHg.
Properties that were predicted by ChemAxon included a topology analysis, which showed an atom count of 25, bond count of 25, cyclomatic number of 1, chain atom count of 7, chain bond count of 7, asymmetric atom count of 1, and rotatable bond count of 3. Under geometry, the information provided showed deriding energy of 28.22 kcal/mol with a volume of 178.72 Å3, a minimal projection area of 35.55 Å2 and maximum at 56.60 Å2.
Chemical and physical properties of compound include a heavy atom count of 16, topological polar surface area of 35.5, covalently bonded unit count of 1, feature 3D hyrdrophobe count of 1, feature 3D ring count of 1, and effective rotor count of 5.
Product Introduction
4-EFMC is a member of the substituted amphetamine, substituted cathinone and substituted methylenedioxyphenethylamine classes.
4-EFMC is the substituted cathinone analog of MDMA and the 3,4-methylenedioxy analog of methcathinone. The only structural difference of methylone with respect to MDMA is the substitution of 2 hydrogen atoms by 1 oxygen atom in the β position of the phenethylamine core, forming a ketone group.
4-EFMC was first synthesized by the chemists Peyton Jacob III and Alexander Shulgin in 1996 for potential use as an antidepressant. Starting around 2004, methylone has been sold for recreational use, taking advantage of the absence of legal prohibition of this compound in many countries.
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