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79233-72-0

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79233-72-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79233-72-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,3 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79233-72:
(7*7)+(6*9)+(5*2)+(4*3)+(3*3)+(2*7)+(1*2)=150
150 % 10 = 0
So 79233-72-0 is a valid CAS Registry Number.

79233-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridine-2-carboxylic acid t-butyl ester

1.2 Other means of identification

Product number -
Other names tert-butyl 2-pyridinecarboxylate

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:79233-72-0 SDS

79233-72-0Relevant articles and documents

Transition-metal catalyzed oxidations. 7. Zirconium-catalyzed oxidation of primary and secondary alcohols with hydroperoxides

Krohn, Karsten,Vinke, Ingeborg,Adam, Horst

, p. 1467 - 1472 (2007/10/03)

A new procedure for the oxidation (dehydrogenation) of primary and secondary alcohols employing Zr(O-t-Bu)4 or Zr(O-n-Pr)4/tert-butyl hydroperoxide/3 A molecular sieves is presented. Secondary alcohols - if not severely sterically hindered - are usually converted quantitatively to the corresponding ketones. Esters or acids can be by products in the reaction of primary alcohols. However, the aldehydes are obtained in good yield by lowering the reaction temperature, decreasing the amount of TBHP or replacing TBHP by cumene hydroperoxide (CHP), and/or exchanging the catalyst Zr(O-t-Bu)4 by Zr(O-n-Pr)4 or silica gel-supported Zr(OR)(x). A remarkable selectivity of equatorial alcohol groups (e.g., 11 and 13) is observed in contrast to chromium(VI)-based oxidations. Strongly chelating substrates such as furfuryl alcohol (18) or 1,2-diol 25 that prevent hydride transfer in the six-membered transition state A are not converted.

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