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4,8-di-tert-butyl-2,10-dimethyl-6-phenoxy-12H-dibenzo[d,g][1,3,2]dioxaphosphocine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34573-99-4

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34573-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34573-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,7 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34573-99:
(7*3)+(6*4)+(5*5)+(4*7)+(3*3)+(2*9)+(1*9)=134
134 % 10 = 4
So 34573-99-4 is a valid CAS Registry Number.

34573-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,9-ditert-butyl-3,7-dimethyl-11-phenoxy-5H-benzo[d][1,3,2]benzodioxaphosphocine

1.2 Other means of identification

Product number -
Other names 4',5"-dimethyl-3",6'-di-tert-butyl-2-phenoxy-4,5,7,8-dibenzo-6H-1,3,2-dioxaphosphocin

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:34573-99-4 SDS

34573-99-4Relevant academic research and scientific papers

Diverse Modes of Reactivity of Dialkyl Azodicarboxylates with P(III) Compounds: Synthesis, Structure, and Reactivity of Products Other than the Morrison-Brunn-Huisgen Intermediate in A Mitsunobu-Type Reaction

Satish Kumar,Praveen Kumar,Pavan Kumar,Kommana, Praveen,Vittal, Jagadese J.,Kumara Swamy

, p. 1880 - 1889 (2004)

The reactivity of diethyl azodicarboxylate (DEAD)/diisopropyl azodicarboxylate (DIAD) with P(III) compounds bearing oxygen or nitrogen substituents is explored. Compounds with structures quite different from that of Morrison-Brunn-Huisgen intermediate R′

Syntheses und NMR-Spektren phosphororganischer Antioxidantien und verwandter Verbindungen

Koenig, T.,Habicher, W.D.,Haehner, U.,Pionteck, J.,Rueger, C.,Schwetlick, K.

, p. 333 - 349 (2007/10/02)

The syntheses of various aliphatic, aromatic, sterically hindered, and cyclic organophosphorus compounds (phosphorous acid esters, esters chlorides and ester amides, hydrogen phosphites, phosphinates and phosphates) are reported, and general procedures for preparation are given.The compounds synthesized were investigated by means of 31P-, 1H- and 13C-n.m.r. spectroscopy, and the chemical shifts measured are listed.

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