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308-95-2

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308-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 308-95-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 308-95:
(5*3)+(4*0)+(3*8)+(2*9)+(1*5)=62
62 % 10 = 2
So 308-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C10F21N/c11-1(12)2(13,14)4(17,18)6(21,5(19,20)3(1,15)16)32(9(28,29)7(22,23)24)10(30,31)8(25,26)27

308-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name perfluoro(diethylcyclohexylamine)

1.2 Other means of identification

Product number -
Other names perfluoro-N,N-diethylcyclohexylamine

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:308-95-2 SDS

308-95-2Downstream Products

308-95-2Relevant articles and documents

ELECTROCHEMICAL FLUORINATION OF SOME CYCLIC TERTIARY AMINES

Conte, L.,Fraccaro, C.,Napoli, M.,Mistrorigo, M.

, p. 183 - 190 (2007/10/02)

Electrochemical fluorination of N,N-diethylcyclohexylamine and N-ethyldicyclohexylamine gave the corresponding F-amines together with several other compounds arising from incomplete fluorination and fragmentation reactions.In the case of N,N-diethylcyclohexylamine yields of 51-52percent were obtained and most of the reaction products were isolated and identified.With N-ethyldicyclohexylamine a lower yield (16percent) was observed; The resultant reaction mixture was too complex to allow the identification of its components.Comments are made about the reaction mechanism, and NMR and IR data are reported for identified compounds.

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