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N,N-dimethyl-1H-indol-5-amine, also known as 5-dimethylaminoindan or DMI, is an organic compound with the chemical formula C11H14N2. It is a derivative of indole, a heterocyclic aromatic organic compound, and features two methyl groups attached to the nitrogen atom. This colorless to pale yellow crystalline solid is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. DMI is known for its reactivity and can participate in a range of chemical reactions, making it a valuable building block in the creation of more complex molecules.

6843-23-8

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6843-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6843-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,4 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6843-23:
(6*6)+(5*8)+(4*4)+(3*3)+(2*2)+(1*3)=108
108 % 10 = 8
So 6843-23-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2/c1-12(2)9-3-4-10-8(7-9)5-6-11-10/h3-7,11H,1-2H3

6843-23-8SDS

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 N,N-dimethyl-1H-indol-5-amine

1.2 Other means of identification

Product number -
Other names 5-Dimethylamino-indol

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:6843-23-8 SDS

6843-23-8Relevant academic research and scientific papers

Catalytic synthesis method of indole compounds

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Paragraph 0024; 0025; 0026; 0027; 0028; 0029; 0030; 0031, (2016/10/10)

The invention discloses a catalytic synthesis method of indole compounds.The method includes the following steps of firstly, conducting stirring reaction on ortho-nitrostyrolene or derivatives of ortho-nitrostyrolene, bis(pinacolato)diboron, alkali and low-grade saturated monohydric alcohol under the atmosphere of nitrogen; secondly, cooling the reaction product in the first step to the room temperature, adding ethyl acetate to be sufficiently mixed, and washing with ethyl acetate after filtering; thirdly, spin-drying low-grade saturated monohydric alcohol in an organic phase of the material obtained in the second step, passing through a silica gel column, and drip washing the silica gel column with eluent composed of petroleum ether and ethyl acetate to obtain pure products, namely, the indole compounds.By means of the method, under the neutral conditions, bis(pinacolato)diboron low in price serves as the raw material, friendly low-grade saturated monohydric alcohol serves as the solvent, the indole compounds are obtained through simple operation, the raw materials are low in price and easy to obtain, efficiency and safety are high, and wide expandability and good industrial application prospects are achieved.

NOVEL INDOLIC DERIVATIVES, THEIR PREPARATION PROCESSES AND THEIR USES IN PARTICULAR AS ANTIBACTERIALS

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Page/Page column 49, (2010/06/19)

The invention relates to the use of at least one compound of the formula (I), in which R and R3 are particularly a hydrogen atom, R1 is particularly a hydrogen atom or a methyl, ethyl or isobutyl mi group, R4, R5, R6 and R7 are independently a hydrogen atony, an alkoxyl group with 1 to 7 carbon atoms or a halogen atom, R2 is a hydrogen atom, an O? group or an OH group, B is an N-GP1 or NRc, group, GP1 being a Boc or Cbz group, and Rc is a hydrogen atom or a methyl or t-butyl group, for preparing a drug for treating conditions associated with bacterial infections, in particular for treating bacterial diseases.

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