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1,2-Ethanediol, 1,2-diphenyl-, dinitrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58286-69-4

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58286-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58286-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58286-69:
(7*5)+(6*8)+(5*2)+(4*8)+(3*6)+(2*6)+(1*9)=164
164 % 10 = 4
So 58286-69-4 is a valid CAS Registry Number.

58286-69-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diphenylethane-1,2-diol,nitric acid

1.2 Other means of identification

Product number -
Other names dl-Hydrobenzoindinitrat

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:58286-69-4 SDS

58286-69-4Downstream Products

58286-69-4Relevant academic research and scientific papers

Preparation of Di- and polynitrates by ring-opening nitration of epoxides by dinitrogen pentoxide (N2O5)

Golding, Peter,Millar, Ross W.,Paul, Norman C.,Richards, David H.

, p. 7037 - 7050 (2007/10/02)

Eighteen epoxides of various kinds were reacted with N2O5 in chlorinated hydrocarbon solvents (principally CH2Cl2) to give vicinal nitrate ester products by a novel ring-opening nitration reaction. The procedure offers easier temperature control and simpler isolation procedures compared with conventional mixed acid nitrations; it also enables selective nitration reactions to be carried out on polyfunctional substrates. The scope and limitations of the reaction, as well as those of an alternative route utilising N2O4 with in situ oxidation of an intermediate nitrite-nitrate, are discussed.

THE STEREOCHEMISTRY OF THE ADDITION REACTIONS OF ALKENYLAROMATIC COMPOUNDS PROMOTED BY CERIUM(IV) AMMONIUM NITRATE AND CERIUM(IV) ACETATE

Baciocchi, Enrico,Rol, Cesare,Sebastiani, Giovanni Vittorio

, p. 285 - 290 (2007/10/02)

The stereochemistry of the addition reactions to cyclic and acyclic alkenylaromatic compounds promoted by cerium(IV) ammonium nitrate in MeCN and by cerium(IV) acetate in AcOH has been investigated.Trans addition is favoured with cyclic substrates whereas

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