Welcome to LookChem.com Sign In|Join Free
  • or
2-(4-fluorophenyl)-2H-indazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81265-90-9

Post Buying Request

81265-90-9 Suppliers

Recommended suppliers

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

81265-90-9 Usage

Chemical class

Indazole cannabinoids

Receptor

CB1 (cannabinoid receptor)

Function

Potent and selective agonist

Affinity

High affinity for the CB1 receptor

Effects

Strong binding and activation of the CB1 receptor

Applications

Research chemical for studying CB1 receptor activation, potential use in pharmaceutical drugs for pain management and neurological disorders

Legal status

Controlled substance in many countries with legal restrictions due to psychoactive properties.

Check Digit Verification of cas no

The CAS Registry Mumber 81265-90-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,6 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81265-90:
(7*8)+(6*1)+(5*2)+(4*6)+(3*5)+(2*9)+(1*0)=129
129 % 10 = 9
So 81265-90-9 is a valid CAS Registry Number.

81265-90-9SDS

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 2-(4-fluorophenyl)indazole

1.2 Other means of identification

Product number -
Other names -

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:81265-90-9 SDS

81265-90-9Downstream Products

81265-90-9Relevant academic research and scientific papers

Room-Temperature, Metal-Free, and One-Pot Preparation of 2H-Indazoles through a Mills Reaction and Cyclization Sequence

Kondo, Masaru,Takizawa, Shinobu,Jiang, Yuzhao,Sasai, Hiroaki

, p. 9866 - 9869 (2019)

The Mills reaction and cyclization of readily available 2-aminobenzyl alcohols and nitrosobenzenes using thionyl bromide provided 2H-indazoles in up to 88 % yields. In the metal-free process, acetic acid played a crucial role for the both Mills reaction and cyclization. A brominated 2H-indazole could also be obtained through the one-pot sequence.

Regioselective C3-H Trifluoromethylation of 2 H-Indazole under Transition-Metal-Free Photoredox Catalysis

Murugan, Arumugavel,Babu, Venkata Nagarjuna,Polu, Ashok,Sabarinathan, Nagaraj,Bakthadoss, Manickam,Sharada, Duddu S.

, p. 7796 - 7803 (2019/06/27)

Trifluoromethyl-substituted heteroarenes are biologically active compounds and useful building blocks. In this sequence, we have developed a visible-light-promoted regioselective C3-H trifluoromethylation of 2H-indazole under metal-free conditions, which

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 81265-90-9