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161152-04-1

3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 161152-04-1 Structure

  • Basic information

    1. Product Name: 3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione
    2. Synonyms: 3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione
    3. CAS NO:161152-04-1
    4. Molecular Formula:
    5. Molecular Weight: 312.433
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 161152-04-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione(161152-04-1)
    11. EPA Substance Registry System: 3-(dimethyl-λ4-sulfanylidene)-1,5-diphenyl-pentane-2,4-dione(161152-04-1)

  • 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: 161152-04-1(Hazardous Substances Data)

161152-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161152-04-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 161152-04:
(8*1)+(7*6)+(6*1)+(5*1)+(4*5)+(3*2)+(2*0)+(1*4)=91
91 % 10 = 1
So 161152-04-1 is a valid CAS Registry Number.

161152-04-1Downstream Products

161152-04-1Relevant articles and documents

Synthesis and evaluation of estrogen agonism of diaryl 4,5- dihydroisoxazoles, 3-hydroxyketones, 3-methoxyketones, and 1,3-diketones: A compound set forming a 4D molecular library

Pulkkinen, Juha T.,Honkakoski, Paavo,Per?kyl?, Mikael,Berczi, Istvan,Laatikainen, Reino

supporting information; experimental part, p. 3562 - 3571 (2009/04/06)

In this paper, the preparation and systematic evaluation of estrogen receptor α (ERα) and estrogen receptor β (ERβ) activities of some diaryl-1,3-diones and their synthetic intermediates, diaryl-4,5-dihydroisoxazoles, diaryl-3-hydroxyketones, diaryl-3-met

3-Unsubstituted 1,5-diaryl-2,4-pentanediones and -4-methoxy-2-pentanones: Synthesis via corresponding 3-hydroxy ketones generated from 2-isoxazolines

Pulkkinen, Juha T.,Vepsaelaeinen, Jouko J.

, p. 8604 - 8609 (2007/10/03)

Aryl acetaldoximes are reacted with allylarenes in the presence of sodium hypochlorite to give 3,5-bis(arylmethyl)-2-isoxazolines which are then converted to 1,5-diaryl-4-hydroxy-2-pentanones by a reductive hydrogenation in the presence of water. These in

A General Route to 3-Unsubstituted 1,5-Diaryl-2,4-pentanediones and -4-Methoxy-2-pentanones

Pulkkinen, Juha,Vepsaelaeinen, Jouko,Laatikainen, Reino

, p. 9749 - 9750 (2007/10/02)

2-Isoxazolines are converted to corresponding 3-hydroxyketones which are used as precursors to produce new 3-unsubstituted 1,5-diaryl-2,4-pentanediones and -4-methoxy-2-pentanones.

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