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4-bromo-N,N-dimethyl-indole-1-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

200418-18-4

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200418-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 200418-18-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,4,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 200418-18:
(8*2)+(7*0)+(6*0)+(5*4)+(4*1)+(3*8)+(2*1)+(1*8)=74
74 % 10 = 4
So 200418-18-4 is a valid CAS Registry Number.

200418-18-4SDS

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 4-bromo-N,N-dimethylindole-1-carboxamide

1.2 Other means of identification

Product number -
Other names 4-BROMO-N,N-DIMETHYL-1H-INDOLE-1-CARBOXAMIDE

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:200418-18-4 SDS

200418-18-4Relevant academic research and scientific papers

Photoredox Catalysis Induced Bisindolylation of Ethers/Alcohols via Sequential C-H and C-O Bond Cleavage

Ye, Lu,Cai, Sai-Hu,Wang, Ding-Xing,Wang, Yi-Qiu,Lai, Lin-Jie,Feng, Chao,Loh, Teck-Peng

supporting information, p. 6164 - 6167 (2017/11/24)

A visible-light-engaged 2-fold site-selective alkylation of indole derivatives with aliphatic ethers or alcohols has been accomplished for easy access to symmetric 3,3′-bisindolylmethane derivatives. The experimental data suggest a sequential photoredox catalysis induced radical addition and proton-mediated Friedel-Crafts alkylation mechanism.

Discovery and evaluation of a series of 3-acylindole imidazopyridine platelet-activating factor antagonists

Curtin, Michael L.,Davidsen, Steven K.,Heyman, H. Robin,Garland, Robert B.,Sheppard, George S.,Florjancic, Alan S.,Xu, Lianhong,Carrera Jr., George M.,Steinman, Douglas H.,Trautmann, Jeff A.,Albert, Daniel H.,Magoc, Terrance J.,Tapang, Paul,Rhein, David A.,Conway, Richard G.,Luo, Gongjin,Denissen, Jon F.,Marsh, Kennan C.,Morgan, Douglas W.,Summers, James B.

, p. 74 - 95 (2007/10/03)

Studies conducted with the goal of discovering a second-generation platelet-activating factor (PAF) antagonist have identified a novel class of potent and orally active antagonists which have high aqueous solubility and long duration of action in animal m

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