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ETHYL 2-ETHOXY-4-IODOBENZOATE is a chemical compound with the molecular formula C10H11IO3. It is an iodine-substituted benzoate ester, consisting of an ethyl ester group attached to a 2-ethoxy-4-iodobenzoate structure. This white to off-white solid has a melting point of about 105-109°C and a characteristic odor. Due to its potential harmful effects if ingested, inhaled, or absorbed through the skin, careful handling is required.

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  • 855868-64-3 Structure
  • Basic information

    1. Product Name: ETHYL 2-ETHOXY-4-IODOBENZOATE
    2. Synonyms: ETHYL 2-ETHOXY-4-IODOBENZOATE
    3. CAS NO:855868-64-3
    4. Molecular Formula: C11H13IO3
    5. Molecular Weight: 320.12359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 855868-64-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 359.3°C at 760 mmHg
    3. Flash Point: 171.1°C
    4. Appearance: /
    5. Density: 1.55g/cm3
    6. Vapor Pressure: 2.4E-05mmHg at 25°C
    7. Refractive Index: 1.561
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ETHYL 2-ETHOXY-4-IODOBENZOATE(CAS DataBase Reference)
    11. NIST Chemistry Reference: ETHYL 2-ETHOXY-4-IODOBENZOATE(855868-64-3)
    12. EPA Substance Registry System: ETHYL 2-ETHOXY-4-IODOBENZOATE(855868-64-3)
  • 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: 855868-64-3(Hazardous Substances Data)

855868-64-3 Usage

Uses

Used in Pharmaceutical Industry:
ETHYL 2-ETHOXY-4-IODOBENZOATE is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, ETHYL 2-ETHOXY-4-IODOBENZOATE serves as an intermediate in the production of various agrochemicals. Its role in this process contributes to the development of effective products for agricultural use.
Used in Dye Manufacturing:
ETHYL 2-ETHOXY-4-IODOBENZOATE is also utilized as an intermediate in the manufacturing of dyes. Its chemical properties make it suitable for creating a range of dye products used in different industries.
Used in Organic Compound Synthesis:
ETHYL 2-ETHOXY-4-IODOBENZOATE is used as a building block in the synthesis of various organic compounds. Its versatility in chemical reactions makes it a valuable component in organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 855868-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,8,6 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 855868-64:
(8*8)+(7*5)+(6*5)+(5*8)+(4*6)+(3*8)+(2*6)+(1*4)=233
233 % 10 = 3
So 855868-64-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H13IO3/c1-3-14-10-7-8(12)5-6-9(10)11(13)15-4-2/h5-7H,3-4H2,1-2H3

855868-64-3SDS

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 Ethyl 2-ethoxy-4-iodobenzoate

1.2 Other means of identification

Product number -
Other names -

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:855868-64-3 SDS

855868-64-3Relevant articles and documents

Cis-imidazolines

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Page/Page column 22, (2008/06/13)

There are presented compounds of the formula or pharmaceutically acceptable salts thereof, wherein Y1, Y2, X1, X2, X3 and R are as described in this application. These compounds are believed to inhibit MDM2-p53 interaction and as such the compounds will have anti-hyperproliferative cellular activity.

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