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(1R,5R)-3-bromo-6,6-dimethylbicyclo[3.1.1]heptan-2-one is a complex organic compound with a unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it belongs to the class of bicyclic compounds. The structure consists of a seven-membered ring with two carbon atoms (C6 and C7) forming a quaternary carbon center, and a methyl group (CH3) attached to each of these carbons. Additionally, there is a bromine atom (Br) attached to the third carbon (C3), and a carbonyl group (C=O) at the second carbon (C2). (1R,5R)-3-bromo-6,6-dimethylbicyclo<3.1.1>-heptan-2-one is characterized by its specific stereochemistry, with the R configuration at both the first (C1) and fifth (C5) carbon atoms. It is an important intermediate in the synthesis of various pharmaceuticals and natural products due to its unique structural features and reactivity.

1610-50-0

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1610-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1610-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1610-50:
(6*1)+(5*6)+(4*1)+(3*0)+(2*5)+(1*0)=50
50 % 10 = 0
So 1610-50-0 is a valid CAS Registry Number.

1610-50-0Upstream product

1610-50-0Downstream Products

1610-50-0Relevant academic research and scientific papers

Synthesis of 5'-((2)H3)-(-)-11-Nor-9-carboxy-Δ9-Tetrahydrocannabinol Methyl Ester Methyl Ether

Tius, Marcus A.,Kannangara, G. S. Kamali

, p. 9173 - 9186 (2007/10/02)

A synthesis of 5'-((2)H3)-(-)-11-nor-carboxy-δ9-tetrahydrocannabinol methyl ester methyl ether (4) has been accomplished from α-bromoenone 10.The key steps are the stereocontrolled cyclobutane ring opening of the cuprate adduct 18 and the cyclization of the cyclohexenyl triflate 21 with excess iodotrimethylsilane to produce Δ9-cylohexenyl triflate 22.An efficient, stereospecific synthesis of optically active (-)-11-nor-9-keto-hexahydrocannabinol (8) has also been accomplished.

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