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103196-99-2

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103196-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103196-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103196-99:
(8*1)+(7*0)+(6*3)+(5*1)+(4*9)+(3*6)+(2*9)+(1*9)=112
112 % 10 = 2
So 103196-99-2 is a valid CAS Registry Number.

103196-99-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-ethyl 2-(4-fluorophenoxy)propionate

1.2 Other means of identification

Product number -
Other names (R)-Ethyl-2-(4-Fluorophenoxy)propionate

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:103196-99-2 SDS

103196-99-2Relevant articles and documents

Fluorinated Lactic Acids: Easily Accessible Reagents for the Analysis of Chiral Compounds by (19)F NMR Spectroscopy. (19)F NMR Separation of the Eight Isomers of Menthol

Heumann, Andreas,Faure, Robert

, p. 1276 - 1279 (1993)

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Topical treatment of cataracts in dogs

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, (2009/04/24)

The topical treatment of cataracts in dogs is a composition having an aldose reductase inhibitor (ARI) in a topical carrier. The ARI is preferably 2R,4S-6-fluoro-2-methyl-spiro[chroman-4,4′-imidazolidine]-2′,5′-dione, referred to as 2R-methyl sorbinil, ha

Process for the production of asymmetric hydantoins

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, (2008/06/13)

An improved process for preparing (4S)-6-fluorospiro-[chroman-4,4''-imidazolidine]-2'',5''-dione (sorbinil) or its (2R)-methyl derivative (2-methylsorbinil) is disclosed herein, starting from p-fluorophenol in each instance. The final products obtained ha

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