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Decane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-heptadecafluoro-10,10-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142502-77-0

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142502-77-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142502-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,0 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142502-77:
(8*1)+(7*4)+(6*2)+(5*5)+(4*0)+(3*2)+(2*7)+(1*7)=100
100 % 10 = 0
So 142502-77-0 is a valid CAS Registry Number.

142502-77-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8-Heptadecafluoro-10,10-dimethoxy-decane

1.2 Other means of identification

Product number -
Other names -

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:142502-77-0 SDS

142502-77-0Downstream Products

142502-77-0Relevant academic research and scientific papers

Synthesis of vicinal perfluoroalkyl enol ethers

Zoghlami,Chehidi,Chaabouni,Baklouti

, p. 1887 - 1892 (2007/10/03)

A convenient preparation of vicinal perfluoroalkyl enol ethers, by the action of alcohols on 1-bromo-1-perfluoroalkylethylenes in the presence of potassium hydroxide, is described. Some aspects of their reactivity are reported.

Synthesis of fluoroalkyl ethanal: R(F)CH2CHO

Laurent,Blancou,Commeyras

, p. 2489 - 2492 (2007/10/02)

Aldehydes R(F)CH2CHO (R(F) is a linear perfluoroalkyl chain) have been obtained in the addition reaction of R(F)I to vinyl acetate in the presence of zinc. R(F)CH2CHIOAc is formed as an intermediate in the course of the reaction. Under appropriate conditions, R(F)CH2CHO and its acylal or acetal derivatives are obtained in good yields.

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