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Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 161423-38-7 Structure
  • Basic information

    1. Product Name: Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI)
    2. Synonyms: Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI)
    3. CAS NO:161423-38-7
    4. Molecular Formula: C9H14N2O
    5. Molecular Weight: 166.22026
    6. EINECS: N/A
    7. Product Categories: OXAZOLE
    8. Mol File: 161423-38-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 251.7±28.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.063±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.59±0.40(Predicted)
    10. CAS DataBase Reference: Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI)(161423-38-7)
    12. EPA Substance Registry System: Isoxazole, 5-methyl-3-(1-methyl-2-pyrrolidinyl)-, (S)- (9CI)(161423-38-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 161423-38-7(Hazardous Substances Data)

161423-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161423-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,4,2 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 161423-38:
(8*1)+(7*6)+(6*1)+(5*4)+(4*2)+(3*3)+(2*3)+(1*8)=107
107 % 10 = 7
So 161423-38-7 is a valid CAS Registry Number.

161423-38-7Downstream Products

161423-38-7Relevant articles and documents

A base promoted multigram synthesis of aminoisoxazoles: Valuable building blocks for drug discovery and peptidomimetics

Chalyk, Bohdan A.,Kandaurova, Inna Y.,Hrebeniuk, Kateryna V.,Manoilenko, Olga V.,Kulik, Irene B.,Iminov, Rustam T.,Kubyshkin, Vladimir,Tverdokhlebov, Anton V.,Ablialimov, Osman K.,Mykhailiuk, Pavel K.

, p. 25713 - 25723 (2016/03/25)

A practical multigram metal free synthesis of isoxazole-containing building blocks from commercially available amino acids was elaborated. The key reaction was a regioselective [3 + 2]-cycloaddition of in situ generated nitrile oxides with alkynes/enamines. The obtained building blocks were used in the preparation of bioactive compounds and peptidomimetics.

Ligands for brain cholinergic channel receptors: Synthesis and in vitro characterization of novel isoxazoles and isothiazoles as bioisosteric replacements for the pyridine ring in nicotine

Garvey,Wasicak,Elliott,Lebold,Hettinger,Carrera,Lin,He,Holladay,Anderson,Cadman,Raszkiewicz,Sullivan,Arneric

, p. 4455 - 4463 (2007/10/02)

Ligands which activate neuronal nicotinic acetylcholine receptors (nAChRs) represent a potential approach for the palliative treatment for the symptoms of memory loss associated with Alzheimer's disease (AD). Based upon this approach, a series of novel 3,

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