54460-96-7 Usage
General Description
1,1'-Oxybis(2-chloropropane), also known as bis(2-chloroisopropyl) ether, is a chemical compound with the molecular formula C6H12Cl2O. It is a colorless, flammable liquid that is primarily used as a solvent in the production of adhesives, coatings, and sealants. However, it is also used as a chemical intermediate in the manufacture of pharmaceuticals and agrochemicals. Exposure to 1,1'-Oxybis(2-chloropropane) can cause irritation to the skin, eyes, and respiratory system, and it is considered to be a potential occupational hazard. Additionally, this compound has been classified as a possible human carcinogen, with evidence suggesting a link to cancer in laboratory animals. Therefore, proper safety precautions and handling procedures should be followed when working with 1,1'-Oxybis(2-chloropropane) to minimize the risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 54460-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,6 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54460-96:
(7*5)+(6*4)+(5*4)+(4*6)+(3*0)+(2*9)+(1*6)=127
127 % 10 = 7
So 54460-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H12Cl2O/c1-5(7)3-9-4-6(2)8/h5-6H,3-4H2,1-2H3
54460-96-7Relevant articles and documents
Three Component Reactions. XVI. Halogenation of Alk-1-enes in the Presence of Ethylene Oxide and Propylene Oxide
Beger, J.,Schiefer, H.,Scheller, D.
, p. 719 - 728 (2007/10/02)
The products of the chlorination of alk-1-enes in the presence of ethylene oxide and propylene oxide were investigated in relation to products of the chlorination in the presence of corresponding chloroalcohols 4 and 5.Isomers dominating in the Markovnikov orientation were found in all cases.Two of the three pairs of diastereomeric bischloropropylethers expected for the chlorination of propene in the presence of propylene oxide were identified by capillar GLC and 13C n.m.r. spectroscopy.
