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2-ISOPROPOXY-[1,3,2]DIOXABORINANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90011-03-3

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90011-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90011-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,1 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90011-03:
(7*9)+(6*0)+(5*0)+(4*1)+(3*1)+(2*0)+(1*3)=73
73 % 10 = 3
So 90011-03-3 is a valid CAS Registry Number.

90011-03-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propan-2-yloxy-1,3,2-dioxaborinane

1.2 Other means of identification

Product number -
Other names 2-Isopropyloxy-<1.3.2>dioxa-borinan

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:90011-03-3 SDS

90011-03-3Downstream Products

90011-03-3Relevant academic research and scientific papers

Synthesis and stability of new spiroaminoborate esters

Stepanenko, Viatcheslav,De Jesús, Melvin,Garcia, Carmelo,Barnes, Charles L.,Ortiz-Marciales, Margarita

experimental part, p. 910 - 913 (2012/03/11)

New spiroaminoborate esters derived from 1,1-diphenylprolinol, ephedrine, and dihydroquinine with different alkoxy substituents were prepared as stable crystalline compounds and characterized by spectroscopical analysis and specific rotation. The structure of the spiroborate 4 derived from 1,1-diphenylprolinol and dicyclohexyl-1,1′-diol was confirmed by X-ray analysis.

Autooxidation of cyclic esters of boric acids

Kuznetsov

, p. 1576 - 1580 (2007/10/03)

1H NMR and IR spectroscopy and mass spectrometry were used to show that the major products of the autooxidation of substituted 1,3,2-dioxaborinanes and 1,3,2-dioxaborolanes upon prolonged handling are the corresponding 2,2′-oxybis(1,3,2-dioxaborinanes) and 2,2′-oxybis(1,3,2-dioxaborolanes). A probable mechanism of this transformation is discussed. 2000 MAIK "Nauka/Interperiodica".

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