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224168-75-6

PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 224168-75-6 Structure

  • Basic information

    1. Product Name: PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL
    2. Synonyms: PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL
    3. CAS NO:224168-75-6
    4. Molecular Formula: C28H23N3O
    5. Molecular Weight: 417.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 224168-75-6.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: PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL(CAS DataBase Reference)
    10. NIST Chemistry Reference: PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL(224168-75-6)
    11. EPA Substance Registry System: PYRIDIN-4-YL(1-TRITYL-1H-IMIDAZOL-4-YL)METHANOL(224168-75-6)

  • 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: 224168-75-6(Hazardous Substances Data)

224168-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 224168-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,4,1,6 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 224168-75:
(8*2)+(7*2)+(6*4)+(5*1)+(4*6)+(3*8)+(2*7)+(1*5)=126
126 % 10 = 6
So 224168-75-6 is a valid CAS Registry Number.

224168-75-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridin-4-yl-(1-tritylimidazol-4-yl)methanol

1.2 Other means of identification

Product number -
Other names AGN-PC-009UVV

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:224168-75-6 SDS

224168-75-6Relevant articles and documents

NOVEL PHARMACEUTICALLY ACCEPTABLE SALTS OF 4-(1H-IMIDAZOL-4-YLMETHYL)PYRIDINE AND THEIR THERAPEUTICAL USES

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Page/Page column 13-14, (2010/12/18)

The present invention concerns novel pharmaceutical compositions of immethridine, in particular of novel pharmaceutically acceptable salts thereof, such as the dioxalate salt of immethridine, as well as its therapeutical uses and novel process of preparation.

Novel histamine H3 receptor antagonists based on the 4-[(1H-imidazol-4-yl)methyl]piperidine scaffold

Vaccaro, Wayne D.,Sher, Rosy,Berlin, Michael,Shih, Neng-Yang,Aslanian, Robert,Schwerdt, John H.,McCormick, Kevin D.,Piwinski, John J.,West Jr., Robert E.,Anthes, John C.,Williams, Shirley M.,Wu, Ren-Long,She, H. Susan,Rivelli, Maria A.,Mutter, Jennifer C.,Corboz, Michel R.,Hey, John A.,Favreau, Leonard

, p. 395 - 399 (2007/10/03)

We report the discovery of novel histamine H3 receptor antagonists based on 4-[(1H-imidazol-4-yl)methyl]piperidine. The most potent compounds in the series (e.g., 7) result from the attachment of a substituted aniline amide to the main pharmaco

Synthesis and Structure-Activity Relationships of Conformationally Constrained Histamine H3 Receptor Agonists

Kitbunnadaj, Ruengwit,Zuiderveld, Obbe P.,De Esch, Iwan J. P.,Vollinga, Roeland C.,Bakker, Remko,Lutz, Martin,Spek, Anthony L.,Cavoy, Emile,Deltent, Marie-France,Menge, Wiro M. P. B.,Timmerman, Henk,Leurs, Rob

, p. 5445 - 5457 (2007/10/03)

Immepip, a conformationally constrained analogue of the histamine congener imbutamine, shows high affinity and functional activity on the human H 3 receptor. Using histamine and its homologues as prototypes, other rigid analogues containing eit

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