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(E)-2-(4-iodo-3-methylbut-3-en-1-yl)-1,3,3-trimethylcyclohex-1-ene is a complex organic compound characterized by its unique molecular structure. It features a cyclohexene ring with three methyl groups attached to the carbon atoms at positions 1, 3, and 3. The compound is further distinguished by a 4-iodo-3-methylbut-3-en-1-yl group at the 2-position of the cyclohexene ring, which introduces a halogenated alkene moiety. This structure endows the compound with specific chemical properties and potential applications in various fields, such as pharmaceuticals or materials science, where its unique combination of functional groups and stereochemistry can be exploited.

74133-09-8

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74133-09-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74133-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,1,3 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 74133-09:
(7*7)+(6*4)+(5*1)+(4*3)+(3*3)+(2*0)+(1*9)=108
108 % 10 = 8
So 74133-09-8 is a valid CAS Registry Number.

74133-09-8Relevant articles and documents

Bidirectional Hiyama–Denmark Cross-Coupling Reactions of Bissilyldeca-1,3,5,7,9-pentaenes for the Synthesis of Symmetrical and Non-Symmetrical Carotenoids

Rivas, Aurea,Pérez-Revenga, Víctor,Alvarez, Rosana,de Lera, Angel R.

supporting information, p. 14399 - 14407 (2019/11/03)

The construction of the carotenoid skeleton by Pd-catalyzed Csp2?Csp2 cross-coupling reactions of symmetrical and non-symmetrical 1,10-bissilyldeca-1,3,5,7,9-pentaenes and the corresponding complementary alkenyl iodides has been developed. Reaction conditions for these bidirectional and orthogonal Hiyama–Denmark cross-coupling reactions of bisfunctionalized pentaenes are mild and the carotenoid products preserve the stereochemical information of the corresponding oligoene partners. The carotenoids synthesized in this manner include β,β-carotene and (3R,3′R)-zeaxanthin (symmetrical) as well as 9-cis-β,β-carotene, 7,8-dihydro-β,β-carotene and β-cryptoxanthin (non-symmetrical).

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