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167354-92-9

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167354-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 167354-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,7,3,5 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 167354-92:
(8*1)+(7*6)+(6*7)+(5*3)+(4*5)+(3*4)+(2*9)+(1*2)=159
159 % 10 = 9
So 167354-92-9 is a valid CAS Registry Number.

167354-92-9Upstream product

167354-92-9Relevant articles and documents

Identification and quantification of the regioisomeric cholesteryl linoleate hydroperoxides in oxidized human low density lipoprotein and high density lipoprotein

Kenar, James A.,Havrilla, Christine M.,Porter, Ned A.,Guyton, John R.,Brown, Spencer A.,Klemp, Keith F.,Selinger, Elizabeth

, p. 737 - 744 (1996)

Oxidation of human LDL is implicated as an initiatior of atherosclerosis. Isolated low density lipoprotein (LDL) and high density lipoprotein (HDL2) were exposed to aqueous radicals generated from the thermolabile azo compound 2,2'-azobis(2-amidinopropane) dihydrochloride. The primary nonpolar lipid products formed from the autoxidation of LDL and HDL were the regioisomeric cholesteryl linoleate hydroperoxides. In LDL oxidations, 9- and 13- hydroperoxides with trans,cis conjugated diene were formed as the major oxidation products if endogenous α-tocopherol was present in the LDL. After extended oxidation of LDL, at the time when endogenous α-tocopherol was consumed, the two trans,cis conjugated diene hydroperoxides began to disappear and the 9- and 13-hydroperoxides with trans,trans conjugated diene appeared. At very long oxidation times, none of the primary products, the conjugated diene hydroperoxides, were present. In HDL2, which has only very low levels of antioxidants, both the 9- and 13-hydroperoxides with trans,cis conjugated diene and the 9- and 13-hydroperoxides with trans,trans conjugated diene were formed at early stages of oxidation. The corresponding alcohols were also formed in the HDL2 oxidations. A mechanistic hypothesis consistent with these observations is presented.

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