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94960-47-1

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94960-47-1 Usage

Usage

UV absorber in various industries

Function

Effective stabilizer for polymers and plastics

Protection

Shields materials from degradation caused by UV radiation

Mechanism

Absorbs and dissipates harmful UV rays

Application

Synthesis of pharmaceuticals

Additional Use

Corrosion inhibitor for metals

Significance

Valuable chemical in material science and industrial applications

Molecular Structure

Unique properties due to its molecular structure

Check Digit Verification of cas no

The CAS Registry Mumber 94960-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,9,6 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94960-47:
(7*9)+(6*4)+(5*9)+(4*6)+(3*0)+(2*4)+(1*7)=171
171 % 10 = 1
So 94960-47-1 is a valid CAS Registry Number.

94960-47-1SDS

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 1-(2-morpholin-4-yl-ethyl)-1H-benzo[1,2,3]triazole

1.2 Other means of identification

Product number -
Other names 1-[2-Morpholino-aethyl]-benzotriazol

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:94960-47-1 SDS

94960-47-1Downstream Products

94960-47-1Relevant articles and documents

Synthesis and muscarinic receptor binding profiles of antagonist benzotriazole derivatives

Cappello,Greco,Novellino,Perissutti,Santagada,Silipo,Vittoria,Di Carlo,Meli,Muccioli

, p. 907 - 918 (2007/10/02)

A series of benzotriazole derivatives were synthesized and tested in order to determine their activities for muscarinic receptor subtypes (M1, M2 and M3). Binding affinities were measured as K1 values by competition against [3H]N-methylscopolamine in rat cortex, atria and ileum. Pharmacological in vitro tests were performed on isolated tissue preparations (rabbit vas deferens, guinea pig atria and ileum); the compounds showed antimuscarinic activity. The synthesized ligands were characterized by moderate activity; however, some of them displayed interesting selectivity profiles (M2/M1 and M2/M3); particularly, the selectivity exhibited by the benzotriazole derivative 14b was quite similar to that observed for AF-DX 116, a typical M2 specific antagonist.

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