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词条 N-Methylpseudoephedrine
释义

  1. References

{{DISPLAYTITLE:N-Methylpseudoephedrine}}{{Chembox
| Name = N-Methylpseudoephedrine
| ImageFile = N-Methylpseudoephedrine.svg
| ImageSize =
| IUPACName = (1S,2S)-2-(Dimethylamino)-1-phenyl-1-propanol
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo = 51018-28-1
| CASNo_Ref = {{cascite|correct|}}
| PubChem = 7059596
| ChemSpiderID = 5415764
| SMILES = O[C@@H](c1ccccc1)[C@@H](N(C)C)C
| InChI = 1/C11H17NO/c1-9(12(2)3)11(13)10-7-5-4-6-8-10/h4-9,11,13H,1-3H3/t9-,11+/m0/s1
| InChIKey = FMCGSUUBYTWNDP-GXSJLCMTBS
| StdInChI = 1S/C11H17NO/c1-9(12(2)3)11(13)10-7-5-4-6-8-10/h4-9,11,13H,1-3H3/t9-,11+/m0/s1
| StdInChIKey = FMCGSUUBYTWNDP-GXSJLCMTSA-N
|Section2={{Chembox Properties
| C=11 | H=17 | N=1 | O=1
| Appearance =
| Density =
| MeltingPtC = 29 to 31
| MeltingPt_ref = [1]
| BoilingPt =
| Solubility =
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}N-Methylpseudoephedrine is a stimulant. It is a derivative of pseudoephedrine and an isomer of N-methylephedrine. It is present in ephedra.[2]

In organic chemistry, it is used in asymmetric synthesis.[1]

References

1. ^(1S,2S)-(+)-N-Methylpseudoephedrine at Sigma-Aldrich
2. ^{{cite book | title = Encyclopedia of International Sports Studies: A-E | author = Roger Bartlet | page = 425 | publisher = Taylor & Francis | year = 2006}}
{{DEFAULTSORT:Methylpseudoephedrine, N-}}

2 : Stimulants|Substituted amphetamines

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