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Benzene, [(1-methoxyethyl)seleno]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137469-49-9

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137469-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137469-49-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,6 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137469-49:
(8*1)+(7*3)+(6*7)+(5*4)+(4*6)+(3*9)+(2*4)+(1*9)=159
159 % 10 = 9
So 137469-49-9 is a valid CAS Registry Number.

137469-49-9SDS

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 1-methoxy-1-(phenylseleno)ethane

1.2 Other means of identification

Product number -
Other names -

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:137469-49-9 SDS

137469-49-9Downstream Products

137469-49-9Relevant academic research and scientific papers

SYNTHETIC APPLICATION OF SELENOSTANNANES: SELENOALKOXYLATION OF ACETALS

Nishiyama, Yutaka,Aoyama, Satoshi,Hamanaka, Sawako

, p. 267 - 270 (2007/10/02)

Monoselenoacetals were easily prepared from the corresponding acetals and tributyltin phenyl selenide (n-Bu3SnSePh) by the action of BF3*Et2O in fair to good yields.

Synthesis of Monoselenoacetals Using Diisobutylaluminium Benzeneselenolate

Nishiyama, Yutaka,Nakata, Shinji,Hamanaka, Sawako

, p. 1775 - 1776 (2007/10/02)

Monoselenoacetals can be synthesized from the reaction of acetals with diisobutylaluminium benzeneselenolate (i-Bu2AlSePh) under mild conditions in good yields.Diselenoacetals are also obtained by traiting acetals with large excess amount of i-Bu2AlSePh.

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