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Rac.-3α-Brom-4aα H-trans-decalon-(2) is a complex organic chemical compound with the molecular formula C10H17BrO. It is a racemic mixture, meaning it consists of equal amounts of both R and S enantiomers. rac.-3α-Brom-4a α H-trans-decalon-(2) features a decalin core, which is a bicyclic structure with two fused cyclohexane rings. The presence of a bromine atom at the 3α position and a hydrogen atom at the 4aα position, along with the trans configuration, gives rac.-3α-Brom-4a α H-trans-decalon-(2) its unique properties. It is primarily used in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Due to its specific stereochemistry and functional groups, rac.-3α-Brom-4aα H-trans-decalon-(2) can be further modified to create a range of derivatives with diverse applications in the chemical industry.

3849-23-8

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3849-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3849-23-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,4 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3849-23:
(6*3)+(5*8)+(4*4)+(3*9)+(2*2)+(1*3)=108
108 % 10 = 8
So 3849-23-8 is a valid CAS Registry Number.

3849-23-8Relevant academic research and scientific papers

Diels-Alder Reactions of Cycloalkenones. 12. Reaction of trans-Δ1,2-3-Octalone with (E)-Piperylene

Angell, E. Charles,Fringuelli, Francesco,Pizzo, Ferdinando,Taticchi, Aldo,Wenkert, Ernest

, p. 1424 - 1426 (2007/10/02)

The Diels-Alder reaction of (E)-piperylene with trans-Δ1,2-3-octalone under aluminum chloride catalysis is described and structure analysis of the adducts by NMR spectroscopy is presented.The diastereofacial selectivity of the reaction is discu

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