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28509-24-2

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28509-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28509-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,0 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28509-24:
(7*2)+(6*8)+(5*5)+(4*0)+(3*9)+(2*2)+(1*4)=122
122 % 10 = 2
So 28509-24-2 is a valid CAS Registry Number.

28509-24-2SDS

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 tert.-butyl-methyl ether

1.2 Other means of identification

Product number -
Other names tert-butyl-methyl ether

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:28509-24-2 SDS

28509-24-2Relevant articles and documents

Reactivities of Carbonyl Compounds in Acid-Catalyzed Hydride Transfer vs. Electron Transfer

Fukuzumi, Shunichi,Fujita, Morifumi

, p. 2059 - 2062 (1991)

Rate constants for acid-catalyzed hydride-transfer reactions from triethylsilane to a series of carbonyl compounds are compared with those for acid-catalyzed electron transfer from the excited state of 2+ to the same series of carbonyl compounds in the presence of HClO4 in acetonitrile at 298 K.

Polymer-supported solution synthesis of oligosaccharides

-

, (2008/06/13)

The present invention provides improved syntheses of oligosacchairdes. In accordance with preferred embodiments, anomeric specificity in such syntheses can be attained using polymer-supported liquid synthetic design with certain novel diether linkers. The present invention also provides novel strategies for capping imcompletely glycosylated hydroxyls.

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