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33834-54-7

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33834-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33834-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,8,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33834-54:
(7*3)+(6*3)+(5*8)+(4*3)+(3*4)+(2*5)+(1*4)=117
117 % 10 = 7
So 33834-54-7 is a valid CAS Registry Number.

33834-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-(4-methoxyphenyl)selenonylbenzene

1.2 Other means of identification

Product number -
Other names di-p-anisyl selenone

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:33834-54-7 SDS

33834-54-7Downstream Products

33834-54-7Relevant articles and documents

A general and efficient method to convert selenides into selenones by using HOF·CH3CN

Potash, Shay,Rozen, Shlomo

, p. 5574 - 5579 (2013/09/12)

A general route for the preparation of selenones (R2SeO 2) is presented. This task is achieved through the quick and high-yielding reaction of selenides (R2Se) with HOF·CH 3CN. The reaction tolerates some elusiv

Efficient trapping of the intermediates in the photooxygenation of sulfides by aryl selenides and selenoxides

Sofikiti, Nikoletta,Rabalakos, Constantinos,Stratakis, Manolis

, p. 1335 - 1337 (2007/10/03)

Aryl selenides and selenoxides trap efficiently the intermediates in the reaction of singlet oxygen with sulfides. In the co-photooxygenation of 1equiv of an aryl selenoxide with 1.3equiv of dimethyl sulfide, the aryl selenone is formed quantitatively. Ar

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