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6-(2,3-dihydro-1H-indol-1-yl)-N,N-dimethylpyridine-3-sulfonamide is a complex organic compound with the molecular formula C15H18N2O2S. It is a derivative of pyridine-3-sulfonamide, featuring a 2,3-dihydro-1H-indol-1-yl group attached at the 6-position. 6-(2,3-dihydro-1H-indol-1-yl)-N,N-dimethylpyridine-3-sulfonamide is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various drugs. Its structure combines the properties of both the indole and pyridine rings, which can lead to a range of biological activities. The compound is also of interest to researchers due to its unique chemical properties and the possibility of exploring its interactions with biological targets.

7065-58-9

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7065-58-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7065-58-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7065-58:
(6*7)+(5*0)+(4*6)+(3*5)+(2*5)+(1*8)=99
99 % 10 = 9
So 7065-58-9 is a valid CAS Registry Number.

7065-58-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Tetrasiloxanol, 7-chloro-1,1,3,3,5,5,7,7-octamethyl-, acetate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7065-58-9 SDS

7065-58-9Downstream Products

7065-58-9Relevant academic research and scientific papers

REACTION OF OCTAMETHYLCYCLOTETRASILOXANE AND PERMETHYLOLIGOSILOXANES WITH ACYL CHLORIDES IN THE PRESENCE OF CoCl2

Basenko, S. V.,Ogorodnikova, E. I.,Vitkovskii, V. Yu.,Mirskov, R. G.,Voronkov, M. G.

, p. 79 - 83 (2007/10/02)

Octamethylcyclotetrasiloxane is cleaved quantitatively by acetyl chloride (1:1 molar ratio) in the presence of anhydrous CoCl2 in acetonitrile at room temperature to form primarily α-chloro-ω-acetoxyoligodimethylsiloxanes nOCOCH3 (n = 0-3; yield, 60-65percent)>.In the presence of an equimolar amount of trimethylacetoxysilane of hexamethyldisiloxane, the major reaction products are α-methyl-ω-acetoxyoligodimethylsiloxanes nOCOCH3 (n = 4-6; yield, 65-70percent)>.

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