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Ethyl 4-({[2-(1H-indol-3-yl)ethyl]carbamothioyl}amino)benzoate is a complex organic compound with the molecular formula C20H20N2O2S. It is a derivative of benzoic acid, featuring an ethyl group attached to the 4-position of the benzene ring. The molecule also contains an indole moiety, which is a heterocyclic aromatic ring system, and a carbamothioyl group, which is a functional group consisting of a carbonyl group (C=O) and a thiocarbonyl group (C=S). ethyl 4-({[2-(1H-indol-3-yl)ethyl]carbamothioyl}amino)benzoate is characterized by its potential biological activity and may be of interest in pharmaceutical research due to its structural features that could interact with various biological targets.

6197-08-6

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6197-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6197-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6197-08:
(6*6)+(5*1)+(4*9)+(3*7)+(2*0)+(1*8)=106
106 % 10 = 6
So 6197-08-6 is a valid CAS Registry Number.

6197-08-6SDS

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 ethyl 4-[2-(1H-indol-3-yl)ethylcarbamothioylamino]benzoate

1.2 Other means of identification

Product number -
Other names bis(2-hydroxy-4-t-butylphenyl)methane

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:6197-08-6 SDS

6197-08-6Downstream Products

6197-08-6Relevant academic research and scientific papers

Magnesium-mediated ortho-Specific Formylation and Formaldoximation of Phenols

Aldred, Robert,Johnston, Robert,Levin, Daniel,Neilan, James

, p. 1823 - 1832 (2007/10/02)

Deprotonation of phenols using magnesium methoxide, followed by distillative removal of free methanol and addition of paraformaldehyde results in ortho-specific magnesium mediated formylation to give the corresponding salicyladehyde magnesium salts, from which the salicylaldehydes can be isolated by acidic work-up.Addition of aq. hydroxylamine sulfate to the salicylaldehyde magnesium salt, in place of the acid work-up, gives the corresponding salicylaldoximes.

Carbonates of acetylenic alcohols

-

, (2008/06/13)

Polymerizable carbonate compounds of the formula: wherein A is an aromatic polycycle, R1 and R2 are independently hydrogen atom or alkyl, and n is 1, 2 or 3, are disclosed. They are useful as a component of nonemanating, self-curing and heat resistant resin compositions.

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