Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15424-14-3

Post Buying Request

15424-14-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

15424-14-3 Usage

Synthesis Reference(s)

Canadian Journal of Chemistry, 53, p. 1333, 1975 DOI: 10.1139/v75-183

Safety Profile

A poison by ingestion. Whenheated to decomposition it emits toxic vapors of NOx andCl-.

Check Digit Verification of cas no

The CAS Registry Mumber 15424-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,2 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15424-14:
(7*1)+(6*5)+(5*4)+(4*2)+(3*4)+(2*1)+(1*4)=83
83 % 10 = 3
So 15424-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H11ClN2/c14-13(11-7-3-1-4-8-11)16-15-12-9-5-2-6-10-12/h1-10,15H/b16-13+

15424-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Phenylbenzenecarbohydrazonoylchloride

1.2 Other means of identification

Product number -
Other names N-phenylbenzenecarbohydrazonoyl chloride

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:15424-14-3 SDS

15424-14-3Relevant articles and documents

Facile synthesis of hydrazonyl halides by reaction of hydrazones with N-halosuccinimide-dimethyl sulfide complex

Patel, Himatkumar V.,Vyas, Kavita A.,Pandey, Sudhanshu P.,Fernandes, Peter S.

, p. 661 - 668 (1996)

A new and convenient method is described for the synthesis of hydrazonyl halides. Hydrazones on treatment with N-chlorosuccinimide-dimethyl sulfide complex result in the formation of the corresponding hydrazonyl chlorides in good yields. Similarly, treatment of hydrazones with N-bromosuccinimide-dimethyl sulfide complex gives the corresponding hydrazonyl bromide under extremely mild conditions.

Versatile approach to densely substituted isoxazolines and pyrazolines: Focus on a quaternary carbon center as a constitutive feature

Abdelli, Abderrahmen,Gharsa, Haythem,Jma?, Momtez,Gaucher, Anne,Efrit, Mohamed Lotfi,M'rabet, Hedi,Prim, Damien

, (2020)

A new family of isoxazolines has been obtained via 1,3-dipolar cycloaddition in good to high yields under mild conditions. Our approach focused on construction of the heterocyclic ring and direct access to a quaternary carbon center at position 5. The met

Synthesis of 3 H-1,2,4-Triazol-3-ones via NiCl2-Promoted Cascade Annulation of Hydrazonoyl Chlorides and Sodium Cyanate

Du, Shiying,Yang, Zuguang,Tang, Jianhua,Chen, Zhengkai,Wu, Xiao-Feng

supporting information, p. 2359 - 2363 (2021/04/05)

A nickel-promoted cascade annulation reaction for the facile synthesis of 3H-1,2,4-triazol-3-ones from readily available hydrazonoyl chlorides and sodium cyanate has been developed. The transformation occurs through a cascade nickel-promoted intermolecular nucleophilic addition-elimination process, intramolecular nucleophilic addition, and a hydrogen-transfer sequence. The method has been successfully applied for the construction of the core skeleton of the angiotensin II antagonist.

Controlled polymerization of styrene in the presence of Blatter’s radicals

Burdyukova, T. O.,Fedorov, A. Yu.,Grishin, I. D.,Kuznetsova, Yu. L.,Lopatin, M. A.,Malysheva, Yu. B.,Polozov, E. Yu.,Vavilova, A. S.,Zaburdaeva, E. A.

, p. 1470 - 1477 (2020/09/23)

Controlled polymerization of styrene (both self-initiated and initiated with azobisisobutyronitrile) in the presence of Blatter’s radical at 125 °C was studied. When using the radical initiator, there is no induction period. On the basis of UV spectroscopy and MALDI massspectrometry studies, it was established that the Blatter radical is completely consumed at the initial stage of the polymerization, inserting into almost all macromolecules. The prepared polystyrene exhibits the ability to reinitialization in post-polymerization and the synthesis of block copolymers.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 15424-14-3