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1300698-74-1

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1300698-74-1 Usage

Functional groups

Two difluoroethyl groups and one difluoroacetate group

Physical state

Liquid

Boiling point

92-94°C

Melting point

-41°C

Density

1.3 g/cm3

Solubility

Soluble in organic solvents such as ethanol, ether, and chloroform

Reactivity

High reactivity

Uses

Building block in the synthesis of other organic compounds, reagent in organic synthesis, production of pharmaceuticals and agrochemicals, and key intermediate in the manufacturing process of several industrial chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1300698-74-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,6,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1300698-74:
(9*1)+(8*3)+(7*0)+(6*0)+(5*6)+(4*9)+(3*8)+(2*7)+(1*4)=141
141 % 10 = 1
So 1300698-74-1 is a valid CAS Registry Number.

1300698-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoroethyl 2,2-difluoroacetate

1.2 Other means of identification

Product number -
Other names 2,2-DIFLUOROETHYL DIFLUOROACETATE

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:1300698-74-1 SDS

1300698-74-1Downstream Products

1300698-74-1Relevant articles and documents

Method for Producing Difluoroacetyl Chloride

-

Paragraph 0086; 0090, (2013/03/26)

A production method of difluoroacetyl chloride according to the present invention includes a chlorination step of bringing a raw material containing at least either a 1-alkoxy-1,1,2,2-tetrafluoroethane or difluoroacetyl chloride into contact with calcium chloride at a reaction enabling temperature. A production method of 2,2-difluoroethyl alcohol according to the present invention includes a catalytic reduction step of causing catalytic reduction of the difluoroacetyl chloride obtained by the above production method. By these methods, the difluoroacetyl fluoride can be efficiently converted to the difluoroacetyl chloride and to the 2,2-difluoroethyl alcohol.

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