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1727-63-5

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1727-63-5 Usage

Type of compound

Halogenated cyclopropane derivative

Halogen atoms present

Chlorine and Fluorine

Usage

a. Reagent in organic synthesis
b. Production of pharmaceuticals
c. Production of agrochemicals

Potential application

Building block for complex molecules

Physical state at room temperature

Colorless liquid

Toxicity

Moderately toxic

Health hazards

Potential health hazards associated with handling and use

Check Digit Verification of cas no

The CAS Registry Mumber 1727-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,2 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1727-63:
(6*1)+(5*7)+(4*2)+(3*7)+(2*6)+(1*3)=85
85 % 10 = 5
So 1727-63-5 is a valid CAS Registry Number.

1727-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-1-fluoro-2,2,3,3-tetramethylcyclopropane

1.2 Other means of identification

Product number -
Other names 1-Chlor-1-fluor-2,2,3,3-tetramethylcyclpropan

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:1727-63-5 SDS

1727-63-5Relevant articles and documents

Burton,Hahnfeld

, p. 828,831 (1977)

Robinson

, p. 1749,1750 (1965)

Reductive addition of trichlorofluoromethane to ketones initiated by the Mg/LiCl system

Hu, Chang-Ming,Tu, Ming-Hu

, p. 9 - 10 (1994)

Reductive addition of trichlorofluoromethane to ketones initiated by the Mg/LiCl system at -20 deg C to -15 deg C gave dichlorofluoromethyl carbinols in moderate yield.

Addition of CFCl3 to aromatic aldehydes via in situ Grignard reaction

Barkakaty, Balaka,Talukdar, Bandana,Lokitz, Bradley S.

, p. 15098 - 15107 (2015/09/21)

Synthetic modification of trichlorofluoromethane (CFCl3) to non-volatile and useful fluorinated precursors is a cost-effective and an environmentally benign strategy for the safe consumption/destruction of the ozone depleting potential of the r

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