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1H-Isoindole-1,3(2H)-dione, 2-[[2-(bromomethyl)phenyl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124016-47-3

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124016-47-3 Usage

Purpose

Antihistamine to alleviate symptoms of allergic reactions

Symptoms relieved

Sneezing, itching, watery eyes, runny nose

Mechanism of action

Blocks the action of histamine

Additional use

Treatment of Parkinson's disease

Dopamine reuptake inhibition

Present

Contraindications

Glaucoma, enlarged prostate, asthma

Side effects

Drowsiness, impaired mental alertness, impaired physical coordination

Caution advised

Exercise caution when using this medication

Check Digit Verification of cas no

The CAS Registry Mumber 124016-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,1 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124016-47:
(8*1)+(7*2)+(6*4)+(5*0)+(4*1)+(3*6)+(2*4)+(1*7)=83
83 % 10 = 3
So 124016-47-3 is a valid CAS Registry Number.

124016-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[[2-(bromomethyl)phenyl]methyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-[2-(bromomethyl)benzyl]isoindoline-1,3-dione

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:124016-47-3 SDS

124016-47-3Relevant academic research and scientific papers

Search for cyclodextrin-based inhibitors of anthrax toxins: Synthesis, structural features, and relative activities

Karginov, Vladimir A.,Nestorovich, Ekaterina M.,Yohannes, Adiamseged,Robinson, Tanisha M.,Fahmi, Nour Eddine,Schmidtmann, Frank,Hecht, Sidney M.,Bezrukov, Sergey M.

, p. 3740 - 3753 (2006)

Recently, using structure-inspired drug design, we demonstrated that aminoalkyl derivatives of β-cyclodextrin inhibited anthrax lethal toxin action by blocking the transmembrane pore formed by the protective antigen (PA) subunit of the toxin. In the prese

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