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Quinolinium, 1-ethyl-2-methyl-, tetrafluoroborate(1-) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21658-58-2

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21658-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21658-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,5 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21658-58:
(7*2)+(6*1)+(5*6)+(4*5)+(3*8)+(2*5)+(1*8)=112
112 % 10 = 2
So 21658-58-2 is a valid CAS Registry Number.

21658-58-2SDS

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 1-Ethyl-2-methylchinolinium-tetrafluoroborat

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2-methylchinoliniumtetrafluoroborat

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:21658-58-2 SDS

21658-58-2Downstream Products

21658-58-2Relevant academic research and scientific papers

Dyeing method using a specific cationic derivative and a compound selected among a specific aldehyde, a specific ketone, a quinone and a di-imino-isoindoline or 3-amino-isoindolone derivative

-

, (2008/06/13)

Compositions, methods, and kits for dyeing at least one keratin fiber, comprising at least one specific cationic compound and at least one compound chosen from specific aldehydes, specific ketones, quinones, diiminoisoindoline derivatives, and 3-aminoisoindolone derivatives, with the proviso that the inventive compositions do not comprise an oxidizing agent.

Syntheses with Aliphatic Dialdehydes, XLIV. Chiral Pentamethine Cyanine Dyes and Heterocycles from Derivatives of (S)-(+)-2-sec-Butylmalonaldehyde

Reichardt, Christian,Budnik, Ulrich

, p. 2023 - 2030 (2007/10/02)

Syntheses and UV/Vis-spectroscopic properties of the chain-substituted, homochiral pentamethine cyanine dyes 16 and 17 are described. 16 and 17 as well as the homochiral five-, six-, and seven-membered heterocycles 11 - 15 are prepared from derivatives (5 and 6) of homochiral (S)-(+)-2-sec-Butylmalonaldehyde (8), the first known chiral malonaldehyde, which in turn is synthesized in a seven-step procedure from homochiral (S)-(-)-2-methyl-1-butanol (1).

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