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CAS

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57709-77-0

4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 57709-77-0 Structure

  • Basic information

    1. Product Name: 4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone
    2. Synonyms: 4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone;4-(4-chlorophenyl)-2-phenylphthalazin-1-one
    3. CAS NO:57709-77-0
    4. Molecular Formula: C20H13ClN2O
    5. Molecular Weight: 332.79
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 57709-77-0.mol

  • Chemical Properties

    1. Melting Point: 164-165 °C
    2. Boiling Point: 498.0±47.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.26±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: -0.66±0.40(Predicted)
    10. CAS DataBase Reference: 4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone(57709-77-0)
    12. EPA Substance Registry System: 4-(4-chlorophenyl)-2-phenyl-1(2H)-phthalazinone(57709-77-0)

  • 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: 57709-77-0(Hazardous Substances Data)

57709-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57709-77-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57709-77:
(7*5)+(6*7)+(5*7)+(4*0)+(3*9)+(2*7)+(1*7)=160
160 % 10 = 0
So 57709-77-0 is a valid CAS Registry Number.

57709-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-2-phenylphthalazin-1-one

1.2 Other means of identification

Product number -
Other names HMS2405A16

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:57709-77-0 SDS

57709-77-0Relevant articles and documents

Ultrasound-promoted regio and chemoselective synthesis of pyridazinones and phthalazinones catalyzed by ionic liquid [bmim]Br/AlCl3

Zare, Leila,Mahmoodi, Nosrat Ollah,Yahyazadeh, Asieh,Nikpassand, Mohammad

experimental part, p. 740 - 744 (2012/05/20)

The first ultrasound-promoted multicomponent synthesis of pyridazinones and phthalazinones from arenes, cyclic anhydrides and ArNHNH2 in the presence of an efficient recyclable catalyst, [bmim]Br/AlCl3, in high yield and short reaction time is reported.

An efficient one-pot synthesis of pyridazinones and phthalazinones using HY-zeolite

Zare, Leila,Mahmoodi, Nosratollah,Yahyazadeh, Asieh,Mamaghani, Manouchehr,Tabatabaeian, Khalil

experimental part, p. 864 - 867 (2011/09/16)

Figure represented. The first one-pot synthesis of pyridazinones and phthalazinones from arenes, cyclic anhydrides, and ArNHNH2 in the presence of efficient recyclable heterogeneous catalyst, HY-zeolite, in high yield and short reaction time is reported.

An efficient chemo- and regioselective three-component synthesis of pyridazinones and phthalazinones using activated KSF

Zare,Mahmoodi,Yahyazadeh,Mamaghani,Tabatabaeian

experimental part, p. 538 - 541 (2011/02/21)

The first three-component and regioselective synthesis of pyridazinones and phthalazinones from arenes, anhydrides and ArNHNH2 in the presence of efficient recyclable heterogeneous catalyst, montmorillonite-KSF, in high yield and short reaction time is reported.

ALKYLATION OF 1-THIOXO-2-PHENYL-4-ARYL-1,2-DIHYDROPHTHALAZINES BY TRIETHYLOXONIUM TETRAFLUOROBORATE

Oparin, D. A.,Yakovlev, S. V.,Pavlova, L. A.

, p. 843 - 846 (2007/10/02)

1-Thioxo-2-phenyl-4-aryl-1,2-dihydrophthalazines are alkylated by triethyloxonium tetrafluoroborate exclusively at the thiocarbonyl group with the formation of the salts of heteroaromatic ions.Hydrolysis of the latters lead to 1-oxo-2-phenyl-4-aryl-1,2-di

ALKYLATION OF 1-0X0-2-PHENYL(METHYL)-4-ARYL(METHYL)-1,2-DIHYDROPHTHALAZINES WITH TRIETHYLOXONIUM FLUOROBORATE

Volynets, N. F.,Samartseva, I. V.,Khramova, I. V.,Pavlova, L. A.

, p. 1342 - 1346 (2007/10/02)

1-Oxo-2-phenyl-4-aryl-1,2-dihydrophthalazines are alkylated by triethyloxonium fluoroborate at the N3 nitrogen atom, forming corresponding 1-oxo-1,2-dihydrophthalazinium tetrafluoroborates.Under the same conditions 1-oxo-2-methyl-4-phenyl(methy

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