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816-26-2

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816-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 816-26-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 816-26:
(5*8)+(4*1)+(3*6)+(2*2)+(1*6)=72
72 % 10 = 2
So 816-26-2 is a valid CAS Registry Number.

816-26-2SDS

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 ethyl 2-fluoropentanoate

1.2 Other means of identification

Product number -
Other names (+-)-2-Fluor-valeriansaeure-ethylester

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:816-26-2 SDS

816-26-2Relevant articles and documents

SARTAN ANALOGUE

-

, (2019/07/23)

The invention concerns a sartan analogue on basis of a sartan which sartan comprises an alkyl group or an alkoxy group, wherein the sartan analogue only differs from the sartan by a replacement of the alkyl group or the alkoxy group or replacement of a methyl residue or a hydrogen residue of the alkyl group or of the alkoxy group by a fluorine atom.

A semi-molten mixture of hexadecyltributylphosphonium bromide and potassium fluoride in the synthesis of organofluorine compounds

Bhadury, Pinaki S.,Raza, Syed K.,Jaiswal, Devendra K.

, p. 115 - 117 (2007/10/03)

A facile and effective reagent system comprising of a semi-molten mixture of hexadecyltributylphosphonium bromide and potassium fluoride has been developed and its scope has been investigated in nucleophilic fluoride exchange with various organohalides. This simple and convenient reagent system provides organofluorine compounds in high yields even with haloesters in which fluoride catalysed elimination is also feasible.

A FACILE PREPARATION OF ETHYL α-FLUOROALKANOATES

Thenappan, Alagappan,Burton, Donald J.

, p. 3641 - 3644 (2007/10/02)

Alkylation of fluorocarboalkoxymethylene tri-n-butylphosphorane followed by hydrolysis provides the title compounds in moderate to good yields.

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