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89929-99-7

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89929-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89929-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,2 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89929-99:
(7*8)+(6*9)+(5*9)+(4*2)+(3*9)+(2*9)+(1*9)=217
217 % 10 = 7
So 89929-99-7 is a valid CAS Registry Number.

89929-99-7SDS

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-[(2-methyl-3-nitrophenyl)methoxy]oxane

1.2 Other means of identification

Product number -
Other names 3-nitro-2-methylbenzenemethanol tetrahydropyranyl 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:89929-99-7 SDS

89929-99-7Relevant articles and documents

Total Synthesis of Nosiheptide

Wojtas, K. Philip,Riedrich, Matthias,Lu, Jin-Yong,Winter, Philipp,Winkler, Thomas,Walter, Sophia,Arndt, Hans-Dieter

, p. 9772 - 9776 (2016/08/10)

Total synthesis of the bismacrocyclic thiopeptide antibiotic nosiheptide was achieved through the assembly of a fully functionalized linear precursor followed by consecutive macrocyclizations. Key features are a critical macrothiolactonization and a mild deprotection strategy for the 3-hydroxypyridine core. The natural product was identical to isolated authentic material in terms of spectral data and antibiotic activity.

Heterocyclic substituted benzyl alcohol, insecticidal ester derivatives, and intermediates

-

, (2008/06/13)

Disclosed and exemplified are insecticidal and acaricidal optionally substituted furylbenzyl, thienylbenzyl, pyrazinylbenzyl, or pyridinzylbenzyl esters of the pyrethroid acids, novel pyrethroid alcohols and other intermediates, and compositions, a method of use and a process for preparation of the esters.

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