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86967-08-0

2-methoxy-N-(prop-2-yn-1-yl)aniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 86967-08-0 Structure

  • Basic information

    1. Product Name: 2-methoxy-N-(prop-2-yn-1-yl)aniline
    2. Synonyms: 2-methoxy-N-(prop-2-yn-1-yl)aniline
    3. CAS NO:86967-08-0
    4. Molecular Formula:
    5. Molecular Weight: 161.203
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 86967-08-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-methoxy-N-(prop-2-yn-1-yl)aniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-methoxy-N-(prop-2-yn-1-yl)aniline(86967-08-0)
    11. EPA Substance Registry System: 2-methoxy-N-(prop-2-yn-1-yl)aniline(86967-08-0)

  • 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: 86967-08-0(Hazardous Substances Data)

86967-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86967-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86967-08:
(7*8)+(6*6)+(5*9)+(4*6)+(3*7)+(2*0)+(1*8)=190
190 % 10 = 0
So 86967-08-0 is a valid CAS Registry Number.

86967-08-0Relevant articles and documents

HETEROCYCLIC COMPOUND

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Paragraph 1688; 1888-1889, (2021/04/02)

The present invention provides a compound having a glucosylceramide lowering action (e.g., promoting glucosylceramide metabolism, inhibition of glucosylceramide synthesis, promoting glucosylceramide catabolism, etc.), which is expected to be useful as an

One-pot preparation of pyrrole derivatives via the copper-catalyzed [4+1] annulation of propargylic amines with ethyl glyoxylate and phenylglyoxal in the presence of piperidine

Sakai, Norio,Suzuki, Hiroki,Hori, Hiroaki,Ogiwara, Yohei

supporting information, p. 63 - 66 (2016/12/23)

We describe how copper(II) chloride efficiently catalyzes the [4+1] annulation of propargylamines with either ethyl glyoxylate or phenylglyoxal functioning as a C1 unit, in the presence of piperidine, which leads to a straightforward and one-pot preparati

AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines

Yuan, Bingxiang,Zhang, Fuming,Li, Zhuomei,Yang, Shenghua,Yan, Rulong

supporting information, p. 5928 - 5931 (2016/11/29)

A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2 through oxidation/cyclization reaction had been developed. AgNO2 was used as the NO source for the first time to synthesize pyrazole N-o

Thiol activated prodrugs of sulfur dioxide (SO2) as MRSA inhibitors

Pardeshi, Kundansingh A.,Malwal, Satish R.,Banerjee, Ankita,Lahiri, Surobhi,Rangarajan, Radha,Chakrapani, Harinath

, p. 2694 - 2697 (2015/06/08)

Drug resistant infections are becoming common worldwide and new strategies for drug development are necessary. Here, we report the synthesis and evaluation of 2,4-dinitrophenylsulfonamides, which are donors of sulfur dioxide (SO2), a reactive sulfur species, as methicillin-resistant Staphylococcus aureus (MRSA) inhibitors. N-(3-Methoxyphenyl)-2,4-dinitro-N-(prop-2-yn-1-yl)benzenesulfonamide (5e) was found to have excellent in vitro MRSA inhibitory potency. This compound is cell permeable and treatment of MRSA cells with 5e depleted intracellular thiols and enhanced oxidative species both results consistent with a mechanism involving thiol activation to produce SO2.

Intramolecular aromatic substitution and amino-claisen rearrangement in substituted N-(2-propynyl)anilines on electron impact

Ramana,Sudha

, p. 1028 - 1033 (2007/10/03)

N-(2-Propynyl)anilines undergo amino-Claisen rearrangement to a minor extent in the ion source, losing a molecule of HCN under electron impact conditions. However, metastable molecular ions with energies closer to threshold undergo Claisen rearrangement g

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