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(3E)-4-(4-iodophenyl)but-3-en-2-one, also known as 4-iodo-α-methylcinnamaldehyde, is an organic compound with the chemical formula C11H9IO. It is a yellow solid that is commonly used in organic synthesis and as a reagent in various chemical reactions. (3E)-4-(4-iodophenyl)but-3-en-2-one is known for its unique structure, which consists of a butenone group substituted with an iodine atom and a phenyl group. It is also known for its aromatic properties and is used in the production of various aromatic compounds and pharmaceuticals. Additionally, it has been studied for its potential applications in the development of new drugs and materials. Overall, (3E)-4-(4-iodophenyl)but-3-en-2-one is a versatile chemical with a wide range of applications in the field of organic chemistry.

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  • 18175-21-8 Structure
  • Basic information

    1. Product Name: (3E)-4-(4-iodophenyl)but-3-en-2-one
    2. Synonyms: (E)-4-(4-Iodophenyl)but-3-en-2-one; 3-Buten-2-one, 4-(4-iodophenyl)-
    3. CAS NO:18175-21-8
    4. Molecular Formula: C10H9IO
    5. Molecular Weight: 272.0823
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18175-21-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 338.9°C at 760 mmHg
    3. Flash Point: 158.8°C
    4. Appearance: N/A
    5. Density: 1.637g/cm3
    6. Vapor Pressure: 9.52E-05mmHg at 25°C
    7. Refractive Index: 1.638
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (3E)-4-(4-iodophenyl)but-3-en-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: (3E)-4-(4-iodophenyl)but-3-en-2-one(18175-21-8)
    12. EPA Substance Registry System: (3E)-4-(4-iodophenyl)but-3-en-2-one(18175-21-8)
  • 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: 18175-21-8(Hazardous Substances Data)

18175-21-8 Usage

Uses

Used in Organic Synthesis:
(3E)-4-(4-iodophenyl)but-3-en-2-one is used as a reagent in organic synthesis for its unique structure and aromatic properties. It is commonly used in the production of various aromatic compounds and pharmaceuticals.
Used in Pharmaceutical Industry:
(3E)-4-(4-iodophenyl)but-3-en-2-one is used as a key intermediate in the synthesis of pharmaceuticals due to its unique structure and reactivity. It has been studied for its potential applications in the development of new drugs and materials.
Used in Chemical Research:
(3E)-4-(4-iodophenyl)but-3-en-2-one is used as a research compound in the field of organic chemistry to study its properties, reactivity, and potential applications in the development of new drugs and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 18175-21-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 5 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18175-21:
(7*1)+(6*8)+(5*1)+(4*7)+(3*5)+(2*2)+(1*1)=108
108 % 10 = 8
So 18175-21-8 is a valid CAS Registry Number.

18175-21-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4-(4-iodophenyl)but-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3-Buten-2-one,4-(4-iodophenyl)

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:18175-21-8 SDS

18175-21-8Relevant articles and documents

RhIII-Catalyzed Synthesis of Highly Substituted 2-Pyridones using Fluorinated Diazomalonate

Das, Debapratim,Sahoo, Gopal,Biswas, Aniruddha,Samanta, Rajarshi

supporting information, p. 360 - 364 (2020/01/25)

A RhIII-catalyzed strategy was developed for the rapid construction of highly substituted 2-pyridone scaffolds using α,β-unsaturated oximes and fluorinated diazomalonate. The reaction proceeds through direct, site-selective alkylation based on migratory insertion and subsequent cyclocondensation. A wide substrate scope with different functional groups was explored. The requirement of fluorinated diazomalonate was explored for this transformation. The developed methodology was further extended with the synthesis of the bioactive compound.

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