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Benzeneseleninic acid, 2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88404-77-7

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88404-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88404-77-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88404-77:
(7*8)+(6*8)+(5*4)+(4*0)+(3*4)+(2*7)+(1*7)=157
157 % 10 = 7
So 88404-77-7 is a valid CAS Registry Number.

88404-77-7SDS

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-methoxybenzeneseleninic acid

1.2 Other means of identification

Product number -
Other names 2-Methoxy-benzolseleninsaeure

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:88404-77-7 SDS

88404-77-7Relevant academic research and scientific papers

Optical resolution and racemization of areneseleninic acids

Shimizu, Toshio,Nakashima, Yusuke,Watanabe, Itaru,Hirabayashi, Kazunori,Kamigata, Nobumasa

, p. 2151 - 2155 (2007/10/03)

Various optically active areneseleninic acids (ArSeO2H; Ar = 4-Me-C6H4; 4-MeO-C6H4; 2-MeO-C6H4; 2-MeOCO-C6H4; 2,4,6-Me3-C6H2/sub

Asymmetric Selenoxide Elimination Leading to Chiral Allenic Sulfones

Komatsu, Naoki,Murakami, Tatsushi,Nishibayashi, Yoshiaki,Sugita, Toshio,Uemura, Sakae

, p. 3697 - 3702 (2007/10/02)

Asymmetric oxidation of some aryl vinyl selenides (3) with Sharpless (A-C), modified Sharpless (D) or Davis oxidants (E-G) resulted in the formation of chiral allenic sulfones 5 of up to 42percent enantiomeric excess (ee) via double asymmetric induction,

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