Welcome to LookChem.com Sign In|Join Free
  • or
ethyl 2-[1-(4-methoxyphenyl)ethylidene]hydrazinecarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25445-81-2

Post Buying Request

25445-81-2 Suppliers

Recommended suppliers

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

25445-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25445-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,4 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25445-81:
(7*2)+(6*5)+(5*4)+(4*4)+(3*5)+(2*8)+(1*1)=112
112 % 10 = 2
So 25445-81-2 is a valid CAS Registry Number.

25445-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-[1-(4-methoxyphenyl)ethylideneamino]carbamate

1.2 Other means of identification

Product number -
Other names p-Methoxyacetophenon-carbethoxyhydrazon

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:25445-81-2 SDS

25445-81-2Relevant academic research and scientific papers

Regio- and stereoselective synthesis of thiazoline derivatives via the thioketene-induced ring expansion of aziridines

Wu, Qiuyue,Xu, Jiaxi

supporting information, p. 2714 - 2717 (2022/03/07)

Metal-free thioketene-induced ring expansion of aziridines gave 4-alkylthiazolines stereospecifically from 2-alkylaziridines through an intramolecular substitution at the less substituted ring carbon and 5-arylthiazolines stereoselectively from 2-arylaziridines via tandem ring cleavage and formation through intimate ion-pair intermediates after nucleophilic addition of aziridines to thioketenes generated from 4-substituted 1,2,3-thiadiazoles in the presence of a base.

Efficient one-pot synthesis of 5-perfluoroalkylpyrazoles by cyclization of hydrazone dianions

Ngo, Thang Ngoc,Ejaz, Syeda Abida,Hung, Tran Quang,Dang, Tuan Thanh,Iqbal, Jamshed,Lecka, Joanna,Sévigny, Jean,Langer, Peter

, p. 8277 - 8290 (2015/08/03)

A highly selective and efficient method for the synthesis of 5-trifluoromethylated and 5-perfluoroalkylated pyrazoles has been developed which relies on the cyclization of hydrazine dianions with ethyl perfluorocarboxylates. The pyrazoles prepared were ev

Electrosynthesis of (E)-Ethenyl-O-ethyl-thiocarbonates

Hess, U.,Schulze, M.

, p. 901 - 908 (2007/10/02)

Electrochemical reductions of 4-aryl- and 4,5-diaryl-1,2,3-thiadiazols (1-5) in acetonitrile/0,1 M tetraalkylammonium-supporting-electrolyte at Hg-cathodes in the presence of ethylchloroformiate (CAE) yield (E)-S-(2-aryl) ethenyl- and S-(1,2-diaryl)etheny

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 25445-81-2