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151772-58-6

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  • 1234 Share on googleShare on favoritesShare on facebookShare on twitterMore Sharing Services NONAFLUORO-3,6-DIOXAHEPTANOIC ACID CAS NO.151772-58-6 CAS NO.151772-58-6

    Cas No: 151772-58-6

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151772-58-6 Usage

Chemical Properties

Liquid

Check Digit Verification of cas no

The CAS Registry Mumber 151772-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,7,7 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151772-58:
(8*1)+(7*5)+(6*1)+(5*7)+(4*7)+(3*2)+(2*5)+(1*8)=136
136 % 10 = 6
So 151772-58-6 is a valid CAS Registry Number.

151772-58-6SDS

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 2,2-difluoro-2-[1,1,2,2-tetrafluoro-2-(trifluoromethoxy)ethoxy]acetic acid

1.2 Other means of identification

Product number -
Other names nonafluoro-3,6-dioxaheptanoic acid

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:151772-58-6 SDS

151772-58-6Upstream product

151772-58-6Downstream Products

151772-58-6Relevant articles and documents

Preparation of fluorinated functional compounds

-

, (2008/06/13)

Fluorinated functional compounds, namely perfluorinated and partially-fluorinated functional compounds, such as perfluorinated and partially-fluorinated carboxylic acids, esters, ketones, alcohols, amides, carboxylic acid fluorides, and derivatives thereof, are prepared by: (a) directly fluorinating a fluorinatable cyclic or acyclic carbonate by contacting the carbonate with fluorine gas in a temperature-controlled reactor to fluorinate the carbonate, and (b) combining the resulting fluorinated carbonate with a reactive nucleophile and allowing the carbonate and the nucleophile to react to form a fluorinated functional derivative of the fluorinated carbonate.

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