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10132-01-1

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10132-01-1 Usage

General Description

1-Chloro-4-phenylphthalazine is a specialized chemical compound. Its molecular formula is C14H10ClN3, and its IUPAC name is 1-chloro-4-phenyl-1H-phthalazin-3-amine. It's a member of the class of phthalazines that involves a phthalazine substituted by a chlorine atom at position 1 and a phenyl group at position 4. It's used in a variety of chemical reactions, often as an intermediate compound. However, like many chemicals, handling of it requires care because of potential hazards. There isn't much publicly available information regarding its uses, environmental impact, or health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 10132-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10132-01:
(7*1)+(6*0)+(5*1)+(4*3)+(3*2)+(2*0)+(1*1)=31
31 % 10 = 1
So 10132-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H11ClN2/c1-10-6-8-11(9-7-10)14-12-4-2-3-5-13(12)15(16)18-17-14/h2-9H,1H3

10132-01-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H33125)  1-Chloro-4-phenylphthalazine, 96%   

  • 10132-01-1

  • 250mg

  • 392.0CNY

  • Detail
  • Alfa Aesar

  • (H33125)  1-Chloro-4-phenylphthalazine, 96%   

  • 10132-01-1

  • 1g

  • 1098.0CNY

  • Detail
  • Alfa Aesar

  • (H33125)  1-Chloro-4-phenylphthalazine, 96%   

  • 10132-01-1

  • 5g

  • 3842.0CNY

  • Detail

10132-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-CHLORO-4-PHENYLPHTHALAZINE

1.2 Other means of identification

Product number -
Other names 1-Chloro-4-phenyl-phthalazine

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:10132-01-1 SDS

10132-01-1Relevant articles and documents

Phthalazine-based VEGFR-2 inhibitors: Rationale, design, synthesis, in silico, ADMET profile, docking, and anticancer evaluations

Khedr, Fathalla,Ibrahim, Mohamed-Kamal,Eissa, Ibrahim H.,Abulkhair, Hamada S.,El-Adl, Khaled

, (2021)

In the designed compounds, a new linker was inserted in the form of fragments with verified VEGFR-2 inhibitory potential, including an α,β-unsaturated ketonic fragment, pyrazole, and pyrimidine. Also, new distal hydrophobic moieties were attached to these

New 1,4-disubstituted phthalazines: Synthesis, structure and herbicidal evaluation

Bele, Constantin,Darabantu, Mircea

, p. 641 - 646 (2003)

The rapid synthesis of eighteen new 1,4-disubstituted phthalazines bearing an aryl or benzyl substituent at C-4 and a variety of aryloxy groups at C-1 is reported; full structural assignments are provided by NMR and MS data together with the biological evaluation for some representative terms of the series.

N-Substituted-4-phenylphthalazin-1-amine-derived VEGFR-2 inhibitors: Design, synthesis, molecular docking, and anticancer evaluation studies

El-Adl, Khaled,Ibrahim, Mohamed-Kamal,Khedr, Fathalla,Abulkhair, Hamada S.,Eissa, Ibrahim H.

, (2020/12/14)

In accordance with the significant impetus of the discovery of potent vascular endothelial growth factor receptor 2 (VEGFR-2) inhibitors, herein, we report the design, synthesis, and anticancer evaluation of 12 new N-substituted-4-phenylphthalazin-1-amine

A novel method for heterocyclic amide-thioamide transformations

Fathalla, Walid,Ali, Ibrahim A. I.,Pazdera, Pavel

supporting information, p. 174 - 181 (2017/02/15)

In this paper, we introduce a novel and convenient method for the transformation of heterocyclic amides into heteocyclic thioamides. A two-step approach was applied for this transformation: Firstly, we applied a chlorination of the heterocyclic amides to afford the corresponding chloroheterocycles. Secondly, the chloroherocycles and N-cyclohexyl dithiocarbamate cyclohexylammonium salt were heated in chloroform for 12 h at 61°C to afford heteocyclic thioamides in excellent yields.

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