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S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127367-07-1 Structure
  • Basic information

    1. Product Name: S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE
    2. Synonyms: S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE
    3. CAS NO:127367-07-1
    4. Molecular Formula: C11H16ClNO2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127367-07-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE(127367-07-1)
    11. EPA Substance Registry System: S-3-(2-METHOXYPHENOXY)-PYRROLIDINE HYDROCHLORIDE(127367-07-1)
  • 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: 127367-07-1(Hazardous Substances Data)

127367-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127367-07-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,3,6 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 127367-07:
(8*1)+(7*2)+(6*7)+(5*3)+(4*6)+(3*7)+(2*0)+(1*7)=131
131 % 10 = 1
So 127367-07-1 is a valid CAS Registry Number.

127367-07-1Upstream product

127367-07-1Downstream Products

127367-07-1Relevant articles and documents

Substituted triazole derivatives as oxytocin antagonists

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Page/Page column 40, (2008/06/13)

The present invention relates to substituted triazoles of formula (I), uses thereof, processes for the preparation thereof and compositions containing said compounds. These inhibitors have utility in a variety of therapeutic areas including sexual dysfunction.

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