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Pyridinium, 1,1',1''-[1,3,5-benzenetriyltris(carbonyloxy-11,1-undecanediyl)]tris-, tribromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104544-20-9

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104544-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104544-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104544-20:
(8*1)+(7*0)+(6*4)+(5*5)+(4*4)+(3*4)+(2*2)+(1*0)=89
89 % 10 = 9
So 104544-20-9 is a valid CAS Registry Number.

104544-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzene 1,3,5-tris(11-pyridiniumundecanyl)tricarboxylate tribromide

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:104544-20-9 SDS

104544-20-9Relevant academic research and scientific papers

Host-Guests Binding by a Simple Detergent Derivative: 'Tentacle Molecules'

Suckling, Colin J.

, p. 661 - 662 (1982)

Benzene 1,3,5-tris(11-pyridiniumundecanyl)tricarboxylate trichloride forms complexes with small aromatic compounds in solution in methanol or acetonitrile and inhibits the chlorination of phenol by protective binding.

SELECTIVE FUNCTIONALISATION-7; CHLORINATION OF AROMATIC COMPOUNDS IN THE PRESENCE OF TENTACLE MOLECULES WITH PYRIDINIUM HEAD GROUPS

Robinson, D. I.,Sherrington, D. C.,Suckling, C. J.

, p. 785 - 792 (2007/10/02)

tris-Pyridiniumalkyl triesters of benzene-1,3,5-tricarboxylic acid 3,6 and 11 carbon atoms in the alkyl chain interact with aromatic substrates, phenol, anisole, diphenyl ether and naphthalene in a manner dependent upon the struture of the substrate.Thus all three tentacle molecules interact with phenol through the pyridinium head group as shown by (1)H NMR (250 MHz) and confirmed by inhibition of chlorination of the bound phenol.The remaining substrates interact but away from the head group; chlorination is also inhibited.In these cases, a contributor to the low reactivity of the substrates to chlorination in the presence of the tentacle molecules is shown to be the unexpected inactivation of the chlorinating agent, t-butyl hypochlorite, by the tentacle molecules.

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