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473659-21-1

DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is a complex organic compound that belongs to the class of tritylimidazoles. It features an imidazole ring, a trityl group (triphenylmethyl), and a phosphonate group, which consists of a phosphorus atom bonded to an oxygen atom and a carbon group. DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is utilized in various chemical reactions due to its intricate structure, but detailed information on its physical properties, hazards, or risks may not be readily accessible, necessitating cautious handling during its application.

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  • 473659-21-1 Structure

  • Basic information

    1. Product Name: DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE
    2. Synonyms: DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE;4-[(Diethoxyphosphoryl)methyl]-1-trityl-1H-imidazole, 4-[(Diethylphosphono)methyl]-1-trityl-1H-imidazole
    3. CAS NO:473659-21-1
    4. Molecular Formula: C27H29N2O3P
    5. Molecular Weight: 460.5
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 473659-21-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 593.7°C at 760 mmHg
    3. Flash Point: 312.9°C
    4. Appearance: /
    5. Density: 1.14g/cm3
    6. Vapor Pressure: 1.93E-13mmHg at 25°C
    7. Refractive Index: 1.582
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE(473659-21-1)
    12. EPA Substance Registry System: DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE(473659-21-1)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 473659-21-1(Hazardous Substances Data)

473659-21-1 Usage

Uses

Used in Chemical Synthesis:
DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is used as a reagent in chemical synthesis for its unique structural properties, which allow it to participate in a variety of reactions and contribute to the formation of new compounds.
Used in Research Applications:
In the field of scientific research, DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is used as a research tool to explore its chemical properties and potential applications in various chemical processes and reactions.
Used in Pharmaceutical Industry:
DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is used as an intermediate in the synthesis of pharmaceutical compounds, leveraging its complex structure to facilitate the creation of new drug molecules.
Used in Material Science:
In material science, DIETHYL (1-TRITYL-1H-IMIDAZOL-4-YL)METHYLPHOSPHONATE is used as a component in the development of new materials, potentially contributing to advancements in areas such as polymers, catalysts, and other advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 473659-21-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,6,5 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 473659-21:
(8*4)+(7*7)+(6*3)+(5*6)+(4*5)+(3*9)+(2*2)+(1*1)=181
181 % 10 = 1
So 473659-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H29N2O3P/c1-3-31-33(30,32-4-2)21-26-20-29(22-28-26)27(23-14-8-5-9-15-23,24-16-10-6-11-17-24)25-18-12-7-13-19-25/h5-20,22H,3-4,21H2,1-2H3

473659-21-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(diethoxyphosphorylmethyl)-1-tritylimidazole

1.2 Other means of identification

Product number -
Other names Diethyl (1-trityl-1H-imidazol-4-yl)methylphosphonate

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:473659-21-1 SDS

473659-21-1Relevant articles and documents

IMPROVEMENT IN THE PRODUCTION OF IMIDAZOLE DERIVATIVES AND NOVEL INTERMEDIATES OF THE DERIVATIVES

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Page 8, (2008/06/13)

The invention provides an improvement in the production of imidazole derivatives including histamine H3 agonist immepip and histamine H3 antagonist VUF4929. Desired imidazole derivatives can be easily obtained in high yield by using

An efficient and convenient synthesis of 4-vinylimidazoles using a novel Horner-Wadsworth-Emmons (HWE) reagent: Synthetic studies toward novel histamine H3-ligands

Harusawa, Shinya,Koyabu, Shuji,Inoue, Yasutoshi,Sakamoto, Yasuhiko,Araki, Lisa,Kurihara, Takushi

, p. 1072 - 1078 (2007/10/03)

A novel Horner-Wadsworth-Emmons (HWE)-type reagent 1 reacted readily with various aldehydes and ketones to produce (E)-vinylimidazoles 2 in good yields. The synthetic utility of 1 was demonstrated by the efficient preparation of four histamine H3 ligands 3 by simple hydrogenation of 2.

INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE

-

, (2008/06/13)

The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting farnesyl-protein transferase and the farnesylation of the oncogene protein Ras

INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE

-

, (2008/06/13)

The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invent

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