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432-23-5

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432-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 432-23-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 432-23:
(5*4)+(4*3)+(3*2)+(2*2)+(1*3)=45
45 % 10 = 5
So 432-23-5 is a valid CAS Registry Number.

432-23-5Relevant articles and documents

Scalable synthesis of the aroma compounds d6-β-ionone and d6-β-cyclocitral for use as internal standards in stable isotope dilution assays

Mosaferi, Shabnam,Jelley, Rebecca E.,Fedrizzi, Bruno,Barker, David

supporting information, (2020/12/02)

C13 Norisoprenoids are important aroma compounds in wine, giving positive attributes to the overall wine aroma even when found at very low levels. β-Ionone is considered one of the most important aroma compounds giving violet, woody and raspberry aromas to wine, fruits and vegetables in which it is found. Due to its potent aroma at low levels, precise analytical methods are desired for its quantification. Stable isotope dilution assay (SIDA) is one of the most important of these methods but requires the use of isotopically labelled standards. Herein, we describe the scalable synthesis of d6-β-ionone and d6-β-cyclocitral, another aroma compound with smokey and fruity notes, starting from the relatively inexpensive deuterated starting material d6-acetone.

Total Synthesis of (+)-Acanthodoral by the Use of a Pd-Catalyzed Metal-ene Reaction and a Nonreductive 5-exo-Acyl Radical Cyclization

Zhang, Liming,Koreeda, Masato

, p. 537 - 540 (2007/10/03)

(Equation presented) The first total synthesis of the antibiotic acanthodoral (1) has been achieved from 3-methyl-2-cyclohexen-1-one in 19 steps in 2.1% overall yield. The synthesis features the use of a Pd-ene reaction in the presence of CO to form the endocyclic alkene 8, a nonreductive acyl radical cyclization reaction, and a ring contraction reaction by the Wolff rearrangement. (+)-Acanthodoral has also been synthesized starting from (+)-S-2,2-dimethyl-6-methylenecyclohexanecarboxylic acid.

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Quirin, Marie Jeanne,Taran, Martine,Delmond, Bernard

, p. 1852 - 1856 (2007/10/03)

δ-Pyronene, a terpenic synthon recently made industrially available from myrcene, has been characterized. It is an excellent raw material for the preparation of numerous intermediates used in the synthesis of perfumes and retinoids. Furthermore, new terpenic compounds including the cyclogeranyl skeleton have been prepared.

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