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171429-43-9

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171429-43-9 Usage

General Description

6-(2,3,3-Trimethylindol-1-yl)-hexanoic acid bromide is a chemical compound with a long hydrocarbon chain and a bromide ion attached to a carboxylic acid functional group. The compound also contains a 2,3,3-trimethylindol-1-yl group, which is a type of aromatic ring structure. 6-(2,3,3-TRIMETHYLINDOL-1-YL)-HEXANOIC ACID BROMIDE is often used in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. The presence of the bromide ion may also indicate that this compound has potential applications in organic and inorganic chemistry, such as in substitution reactions or as a source of bromine atoms in other chemical reactions. Overall, 6-(2,3,3-Trimethylindol-1-yl)-hexanoic acid bromide is a versatile compound with potential uses in pharmaceuticals and other chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 171429-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,4,2 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171429-43:
(8*1)+(7*7)+(6*1)+(5*4)+(4*2)+(3*9)+(2*4)+(1*3)=129
129 % 10 = 9
So 171429-43-9 is a valid CAS Registry Number.

171429-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2,3,3-trimethylindol-1-ium-1-yl)hexanoic acid,bromide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:171429-43-9 SDS

171429-43-9Downstream Products

171429-43-9Relevant articles and documents

Verification and biophysical characterization of a new three-color Foerster resonance-energy-transfer (FRET) system in DNA

Kienzler, Andrea Altevogt Nee,Flehr, Roman,Gehne, Soeren,Kumke, Michael U.,Bannwarth, Willi

, p. 543 - 555 (2012)

We report on a new three-color FRET system consisting of three fluorescent dyes, i.e., of a carbostyril (= quinolin-2(1H)-one)-derived donor D, a (bathophenanthroline)ruthenium complex as a relay chromophore A1, and a Cy dye as A2 (FRET = Foerster resonance-energy-transfer) (cf. Fig. 1). With their widely matching spectroscopic properties (cf. Fig. 2), the combination of these dyes yielded excellent FRET efficiencies. Furthermore, fluorescence lifetime measurements revealed that the long fluorescence lifetime of the Ru complex was transferred to the Cy dye offering the possibility to measure the whole system in a time-resolved mode. The FRET system was established on double-stranded DNA (cf. Fig. 3) but it should also be generally applicable to other biomolecules.

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