Welcome to LookChem.com Sign In|Join Free
  • or
Benzenamine, 4-bromo-N-[(2,4-dichlorophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14632-35-0

Post Buying Request

14632-35-0 Suppliers

Recommended suppliers

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

14632-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14632-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,3 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14632-35:
(7*1)+(6*4)+(5*6)+(4*3)+(3*2)+(2*3)+(1*5)=90
90 % 10 = 0
So 14632-35-0 is a valid CAS Registry Number.

14632-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-bromophenyl)-1-(2,4-dichlorophenyl)methanimine

1.2 Other means of identification

Product number -
Other names N-(2.4-Dichlor-benzyliden)-4-brom-anilin

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:14632-35-0 SDS

14632-35-0Relevant academic research and scientific papers

Synthesis and characterization of tetrachloro-1,3-oxazepine derivatives and evaluation of their biological activities

Kshash, Abdullah Hussein

, p. 113 - 118 (2020/04/01)

6,7,8,9-Tetrachloro[1,3]oxazepine-1,5-dione derivatives 1b-10b have been synthesized by reacting Schiff bases 1a-10a with tetrachlorophthalic anhydride (TCPA) under (2 + 5 → 7) cycloaddition reaction conditons. All reactions had been monitored using TLC.

Ir-Catalyzed C?H Amidation of Aldehydes with Stoichiometric/Catalytic Directing Group

Zhang, Yun-Fei,Wu, Bin,Shi, Zhang-Jie

supporting information, p. 17808 - 17812 (2016/11/28)

Ir-catalyzed sp2C?H amidation of aldehydes with various anilines as stoichiometric or catalytic directing groups was accomplished. A wide range of substrates were selectively amidated in good to excellent yields with broad functional group tolerance. The iridacycle complexes were isolated, characterized, and proved as key intermediates. Kinetic studies and Hammett plots provided detailed understandings of this amidation. According to the mechanism, the electron-rich ArSO2N3was proved effective for intermolecular sp3C?H amidation.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 14632-35-0