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372-55-4

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372-55-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 372-55-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 372-55:
(5*3)+(4*7)+(3*2)+(2*5)+(1*5)=64
64 % 10 = 4
So 372-55-4 is a valid CAS Registry Number.

372-55-4SDS

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 2,2-difluoroethyl ethyl ether

1.2 Other means of identification

Product number -
Other names 2-ethoxy-1,1-difluoro-ethane

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:372-55-4 SDS

372-55-4Downstream Products

372-55-4Relevant articles and documents

The preparation of HCF2CdX and HCF2ZnX via direct insertion into the carbon halogen bond of CF2HY (Y = Br, I)

Burton, Donald J.,Hartgraves, Greg A.

, p. 1198 - 1215 (2008/02/08)

The difluoromethylcadmium and zinc reagents have been prepared in DMF via direct insertion of Cd0 into the carbon halogen bond of CF2HY (Y = Br, I). These reagents are stable at 65-75 °C and exhibit prolonged stability and activity at room temperature. Metathesis of the difluoromethylcadmium reagents with Cu(I)X (X = Br, Cl) at -55 °C rapidly produces difluoromethylcopper. The copper reagent is significantly less stable than the cadmium or zinc reagent and rapidly decomposes at room temperature. The difluoromethylcadmium and copper reagents exhibit good reactivity with allylic halides, propargylic derivatives and 1-iodoalkynes to provide good yields of the corresponding difluoromethylalkenes, difluoromethylallenes and difluoromethyl-2-alkynes. Alkylation is successful only with reactive alkyl halides. Generally, the difluoromethylcopper reagent is more reactive than the difluoromethylcadmium reagent and generally exhibits higher regioselectivity in reactions that can occur by either α- or γ-attack.

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