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1H-Isoindole-1,3(2H)-dione, 2-[2-fluoro-2-[(4-methoxyphenyl)sulfinyl]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94404-37-2

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94404-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94404-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,4,0 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94404-37:
(7*9)+(6*4)+(5*4)+(4*0)+(3*4)+(2*3)+(1*7)=132
132 % 10 = 2
So 94404-37-2 is a valid CAS Registry Number.

94404-37-2SDS

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 N-[2-[2-fluoro-(4-methoxyphenyl)sulfinyl]ethyl]phthalimide

1.2 Other means of identification

Product number -
Other names 2-[2-Fluoro-2-(4-methoxy-benzenesulfinyl)-ethyl]-isoindole-1,3-dione

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:94404-37-2 SDS

94404-37-2Downstream Products

94404-37-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of 1-(2-fluorovinyl)-7-substituted-4- quinolone-3-carboxylic acid derivatives, conformationally restricted analogues of fleroxacin

Asahina, Yoshikazu,Iwase, Kazuhiko,Iinuma, Fujio,Hosaka, Masaki,Ishizaki, Takayoshi

, p. 3194 - 3202 (2007/10/03)

The novel 1-(2-fluorovinyl)-4-quinolone-3-carboxylic acid derivatives Z-15a-c, E-15a-c, Z-16a-c, and E-16a-c, conformationally restricted analogues of fleroxacin (5), were synthesized, and their in vitro antibacterial activity was evaluated. A dehydrosulf

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