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17480-54-5

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17480-54-5 Usage

Physical state

Colorless liquid

Odor

Sweet, chloroform-like

Usage

Chemical intermediate in the synthesis of various organic compounds

Flammability

Flammable

Hazardous properties

Forms explosive peroxides

Toxicity

Toxic if ingested, inhaled, or absorbed through the skin

Applications

Production of agrochemicals, pharmaceuticals, and specialty chemicals

Irritation

Known irritant to eyes, skin, and respiratory system

Safety measures

Handle with caution and appropriate safety measures

Check Digit Verification of cas no

The CAS Registry Mumber 17480-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,8 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17480-54:
(7*1)+(6*7)+(5*4)+(4*8)+(3*0)+(2*5)+(1*4)=115
115 % 10 = 5
So 17480-54-5 is a valid CAS Registry Number.

17480-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dichloro-2-prop-1-en-2-ylcyclopropane

1.2 Other means of identification

Product number -
Other names 2,2-Dichlor-1-isopropenyl-cyclopropan

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:17480-54-5 SDS

17480-54-5Downstream Products

17480-54-5Relevant articles and documents

REGIOSPECIFICITY IN THE NUCLEOPHILIC RING OPENING REACTIONS OF gem-DICHLOROCYCLOPROPYLCARBINYL CATIONS

DeWeese, F. Thane,Minter, David E.,Nosovitch, John T.,Rudel, Michael G.

, p. 239 - 244 (2007/10/02)

gem-Dichlorocyclopropylcarbinyl cations, generated under acidific conditions from the corresponding alcohol or alkene, undergo ring opening by nucleophilic attack exclusively at the halogenated carbon when the alternative electrophilic ring carbon is unsubstituted.In one case, a novel trifluoroacetoxydichloromethyl function has been produced and characterized as a masked carboxylic acid chloride.

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