Welcome to LookChem.com Sign In|Join Free
  • or
3H-Naphtho[2,1-b]pyran-3-one, 2-[1-(phenylhydrazono)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

107096-91-3

Post Buying Request

107096-91-3 Suppliers

Recommended suppliers

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

107096-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107096-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107096-91:
(8*1)+(7*0)+(6*7)+(5*0)+(4*9)+(3*6)+(2*9)+(1*1)=123
123 % 10 = 3
So 107096-91-3 is a valid CAS Registry Number.

107096-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-2-(1-(2-phenylhydrazono)ethyl)-3H-benzo[f]chromen-3-one

1.2 Other means of identification

Product number -
Other names 2-[1-(Phenyl-hydrazono)-ethyl]-benzo[f]chromen-3-one

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:107096-91-3 SDS

107096-91-3Relevant academic research and scientific papers

Hydrazone compound and preparation method thereof, ion recognition receptor and applications

-

Paragraph 0029-0031; 0043-0047; 0051-0061, (2020/12/15)

The invention relates to the field of chemistry, and particularly discloses a hydrazone compound and a preparation method thereof, an ion recognition receptor and applications, wherein the hydrazone compound has the following structure described in the sp

Synthesis, anticancer activity and photophysical properties of novel substituted 2-oxo-2H-chromenylpyrazolecarboxylates

Kumar, J. Ashok,Saidachary,Mallesham,Sridhar,Jain, Nishant,Kalivendi, Shashi Vardhan,Rao, V. Jayathirtha,Raju, B. China

, p. 389 - 402 (2013/10/01)

2-Oxo-2H-chromenylpyrazolecarboxylates (8a-h and 12a-zb) have been synthesized by [3 + 2] cycloaddition of 2H-chromenophenylhydrazones (7a-h and 11a-w) with diethyl/dimethylbut-2-ynedioates. Phenylchromeno[4,3-c]pyrazol-4(1H) -ones (13i-n) were prepared from corresponding phenylhydrazones (7a-h) with catalytic amount of piperidine in presence of pyridine as a solvent at 100°C. All the synthesized compounds (8a-h, 12a-zb and 13a-n) were screened for anticancer activity against three human cancer cell lines such as prostate (DU-145), lung adenocarcinoma (A549), and cervical (HeLa) by standard MTT assay method. Further, photophysical properties (UV and fluorescence) for these compounds were discussed.

Synthesis and antimicrobial activity of novel benzo[f]coumarin compounds

Zaki,Elossaily,Kamal El-Dean

, p. 639 - 646 (2013/02/23)

The acetyl benzo[f]coumarin condensed with phenyl hydrazine to afford the corresponding phenyl hydrazone which cyclized into the pyrazolyl benzocoumarin under Vilsmeier reaction conditions. The pyrazolylaldehyde was used as starting material for synthesis

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 107096-91-3