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Trifluoromethanesulfonic acid 4-methoxy-2-nitrophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213596-32-8

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213596-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213596-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,5,9 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 213596-32:
(8*2)+(7*1)+(6*3)+(5*5)+(4*9)+(3*6)+(2*3)+(1*2)=128
128 % 10 = 8
So 213596-32-8 is a valid CAS Registry Number.

213596-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-2-nitrophenyl trifluoromethanesulfonate

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:213596-32-8 SDS

213596-32-8Relevant academic research and scientific papers

Carbazole compounds and therapeutic uses of the compounds

-

, (2015/09/28)

Compounds of the general structural formula (I) and (II) and use of the compounds and salts and hydrates thereof, as therapeutic agents are disclosed. Treatable diseases and conditions include cancers, inflammatory diseases and conditions, and immunodeficiency diseases. (I), (II).

Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

Holzapfel, Cedric W.,Dwyer, Catherine

, p. 1513 - 1518 (2007/10/03)

The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

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