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21654-46-6

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21654-46-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21654-46-6 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 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21654-46:
(7*2)+(6*1)+(5*6)+(4*5)+(3*4)+(2*4)+(1*6)=96
96 % 10 = 6
So 21654-46-6 is a valid CAS Registry Number.

21654-46-6SDS

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 1,2,3,3-tetramethyl-3H-indolium tetrafluoroborate

1.2 Other means of identification

Product number -
Other names 1,2,3,3,-tetramethylindoliniumtetrafluoroborat

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:21654-46-6 SDS

21654-46-6Upstream product

21654-46-6Relevant articles and documents

Synthesis and Properties of β-Phospha-trimethinecyanine Dyes with Indoline End Groups

Gamon, Norbert,Reichardt, Christian

, p. 2072 - 2094 (2007/10/02)

Reaction of 1,3,3-trialkyl-2-methyleneindolines 4 and 5 with phosphorus(III) halides yields, by a twofold nucleophilic substitution, the halogeno-phosphanes 6a-c, which in turn react with trimethyloxonium tetrafluoroborate to give the β-phospha-trimethinecyanine dyes 3a, b.These β-phospha-cyanines 3a, b are the first higher-methinylogous representatives of the phosphamonomethinecyanine dyes 1, synthesized in 1964 by Dimroth and Hoffmann as the first compounds containing phosphorus in the oxidation state +3 and with coordination number 2. - The 1H-, 13C-, 31P-NMR- as well as the UV/VIS spectra of these β-phospha-cyanines 3a, b and of the analogous β-"carba"-, β-aza- and β-arsa-trimethinecyanines are discussed with respect to their constitution, configuration, and ?-electron-density distribution.

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