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"5,6,7,8,9,9-Hexachlor-1,2,3,4,4a,5,8,8a-octahydro-1,4-endo,endo-5,8-dimethanonaphthalin" is a complex organic compound with a highly chlorinated structure. It is composed of an octahydro-napthalene ring system, which is a type of hydrocarbon with eight hydrogen atoms attached to a naphthalene backbone. The compound is characterized by the presence of six chlorine atoms at various positions, which significantly alter its chemical properties. This specific arrangement of chlorine atoms and the partially saturated ring structure contribute to its unique chemical and physical characteristics. Due to its complexity, 5,6,7,8,9,9-Hexachlor-1,2,3,4,4a,5,8,8a-octahydro-1,4-endo,endo-5,8-dimethanonaphthalin is not commonly found in nature and is typically synthesized for specific industrial applications, such as in the production of certain types of chemicals or as an intermediate in chemical reactions.

5669-34-1

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5669-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5669-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5669-34:
(6*5)+(5*6)+(4*6)+(3*9)+(2*3)+(1*4)=121
121 % 10 = 1
So 5669-34-1 is a valid CAS Registry Number.

5669-34-1Relevant academic research and scientific papers

Carbon-13 NMR Spectra of Tetracyclododecanes: Evidence for Upfield δ and ε Steric Effects

Seidl, Peter Rudolf,Leal, Katia Zaccur,Costa, Valentim Emilio Uberti,Moellmann, Maria Elisabeth Stapoel.

, p. 241 - 246 (1993)

13C NMR spectra of 36 endo-endo, exo-endo and exo-exo tetracyclic fused norbornyl compounds are interpreted.Stereochemical influences on 1H and 13C chemical shifts are compared and discussed.Only upfield δ and ε effects are observed. KEY WORDS: Upfield δ and ε effects, 13C chemical shifts, Tetracyclododecane derivatives

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