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14711-91-2

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14711-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14711-91-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,1 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14711-91:
(7*1)+(6*4)+(5*7)+(4*1)+(3*1)+(2*9)+(1*1)=92
92 % 10 = 2
So 14711-91-2 is a valid CAS Registry Number.

14711-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4,4,6,6-HEXAKIS-(4-NITRO-PHENOXY)-,,-(1,3,5,2,4,6)TRIAZATRIPHOSPHININE

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:14711-91-2 SDS

14711-91-2Upstream product

14711-91-2Relevant articles and documents

Tris(o-phenylenedioxy)cyclotriphosphazene as a Promoter for the Formation of Amide Bonds between Aromatic Acids and Amines

Movahed, Farzaneh Soleymani,Sawant, Dinesh N.,Bagal, Dattatraya B.,Saito, Susumu

, p. 3253 - 3262 (2020/11/02)

The atom-efficient formation of amide bonds has emerged as a top-priority research field in organic synthesis, as amide bonds constitute the backbones of proteins and represent an important structural motif in drug molecules. Currently, the increasing demand for novel discoveries in this field has focused substantial attention on this challenging subject. Herein, the degradable 1,3,5-triazo-2,4,6-triphosphorine (TAP) motif is presented as a new condensation system for the dehydrative formation of amide bonds between diverse combinations of aromatic carboxylic acids and amines. The underlying reaction mechanism was investigated, and potential catalyst intermediates were characterized using 31 P NMR spectroscopy and ESI mass spectrometry.

Reactions of phosphonitrilic chloride with p-nitrophenol

Kober, Ehrenfried,Lederle, Henry,Ottmann, Gerhard

, p. 2239 - 2240 (2007/10/13)

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