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437-15-0

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437-15-0 Usage

General Description

Tritylium hexafluoroarsenate is a chemical compound with the formula (C19H15)AsF6. It is an arsenic-containing salt that is commonly used as a strong Lewis acid in organic synthesis. It is a stable and non-hygroscopic compound that is well-suited for reactions requiring a strong acid catalyst, such as Friedel-Crafts acylation and alkylation. Tritylium hexafluoroarsenate is also used as a reagent for the synthesis of various organic compounds and as a catalyst in the production of dyes and pharmaceuticals. Its stable and versatile nature makes it a valuable tool in the realm of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 437-15-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 437-15:
(5*4)+(4*3)+(3*7)+(2*1)+(1*5)=60
60 % 10 = 0
So 437-15-0 is a valid CAS Registry Number.
InChI:InChI=1/C19H15.AsF6/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;2-1(3,4,5,6)7/h1-15H;/q-4;-1

437-15-0SDS

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 diphenylmethylbenzene,hexafluoroarsenic(1-)

1.2 Other means of identification

Product number -
Other names Triphenylmethyl hexafluoroarsenate

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:437-15-0 SDS

437-15-0Relevant articles and documents

Synthesis and structure of tritylium salts

Hinz, Alexander,Labbow, René,Rei?, Fabian,Schulz, Axel,Sievert, Katharina,Villinger, Alexander

, p. 1641 - 1650 (2015/10/28)

Several tritylium compounds [Ph3C][A] have been isolated by salt metathesis or halide abstraction reactions starting from Ph3C-X (X = halogen) and Lewis acids in good yields (A = BF4, BCl4, AlCl4, GaCl4, PF6, AsF6, SbF6, SbCl6, CHB11H5Cl6, CHB11Cl11, CHB11H5Br6, CF3COO, CF3SO3, N3). The structures of 15 tritylium salts bearing different types of weakly coordinating anions (A-) have been determined. The structures are discussed on the basis of ion pairing versus covalent bond formation and solid-state interactions in comparison with gas-phase data.

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