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1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104941-05-1 Structure
  • Basic information

    1. Product Name: 1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one
    2. Synonyms: 2-propen-1-one, 1,2-bis(2,4-dichlorophenyl)-
    3. CAS NO:104941-05-1
    4. Molecular Formula: C15H8Cl4O
    5. Molecular Weight: 346.0354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104941-05-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 481.4°C at 760 mmHg
    3. Flash Point: 202.1°C
    4. Appearance: N/A
    5. Density: 1.427g/cm3
    6. Vapor Pressure: 1.99E-09mmHg at 25°C
    7. Refractive Index: 1.618
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one(104941-05-1)
    12. EPA Substance Registry System: 1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one(104941-05-1)
  • 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: 104941-05-1(Hazardous Substances Data)

104941-05-1 Usage

Physical state at room temperature

Yellow solid

Solubility in water

Insoluble

Usage

Pesticide

Mode of action

Disrupts the nervous system of insects

Toxicity

Toxic to humans

Potential health effects

Causes irritation to skin, eyes, and respiratory system

Safety precautions

Follow all safety guidelines and regulations when handling

Check Digit Verification of cas no

The CAS Registry Mumber 104941-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,9,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 104941-05:
(8*1)+(7*0)+(6*4)+(5*9)+(4*4)+(3*1)+(2*0)+(1*5)=101
101 % 10 = 1
So 104941-05-1 is a valid CAS Registry Number.

104941-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-bis(2,4-dichlorophenyl)prop-2-en-1-one

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:104941-05-1 SDS

104941-05-1Relevant articles and documents

Synthesis and Antifungal Activity of a Series of Novel 1,2-Disubstituted Propenones

Ogata, Masaru,Matsumoto, Hiroshi,Kida, Shiro,Shimizu, Sumio,Tawara, Katsuya,Kawamura, Yoshimi

, p. 1497 - 1502 (2007/10/02)

To find an antifungal agent other than those of the imidazole and triazole series, a new class of 1,2-disubstituted propenones I and II was prepared and tested for antifungal activity.Comparison of the structure-activity relationships showed that the conjugated structure of carbonyl and exomethylene groups in I and II plays an important role in potent antifungal acivity.However, it is noteworthy that compounds 53, 54, and 56, which have a hydroxymethyl or methoxymethyl group instead of an exo-methylene group in I, also showed potent activity.Although many compounds exhibited strong antifungal activity in vitro, none showed activity in vivo of oral efficacy against subacute systemic candidiasis in mice. '

A CONVENIENT SYNTHESIS OF 1H-1,2,4-TRIAZOL-1-YL-PROPAN-3-ONE DERIVATIVES BY MODIFIED MANNICH REACTION

Takahashi, Kimio,Shimizu, Sumio,Ogata, Masaru

, p. 809 - 816 (2007/10/02)

1H-1,2,4-Triazol-yl-propan-3-ones were synthesized regioselectively using a modified Mannich reaction.Reactions of enones and Mannich bases with imidazole are also described.

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