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1,7,7-trimethyl-2-phenylbicyclo[2.2.1]heptan-2-exo-ol is a complex organic compound with the molecular formula C16H22O. It is a bicyclic molecule, featuring a seven-membered ring with two methyl groups attached to the first carbon and one methyl group attached to the seventh carbon. The phenyl group is connected to the second carbon of the bicyclic structure. The exo-ol indicates that the hydroxyl group (-OH) is located on the exterior of the molecule, specifically on the second carbon of the bicyclic ring. 1,7,7-trimethyl-2-phenylbicyclo<2.2.1>heptan-2-exo-ol is known for its unique structure and potential applications in the synthesis of various pharmaceuticals and fragrances.

7070-01-1

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7070-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7070-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7070-01:
(6*7)+(5*0)+(4*7)+(3*0)+(2*0)+(1*1)=71
71 % 10 = 1
So 7070-01-1 is a valid CAS Registry Number.

7070-01-1Relevant academic research and scientific papers

Improved addition of phenyllithium to hindered ketones by the use of non-polar media

Lecomte, Vincent,Stéphan, Elie,Jaouen, Gérard

, p. 3463 - 3465 (2007/10/03)

The use of a non-polar medium at room temperature is an efficient, cheap and easy way to improve the low reactivity of six hindered ketones towards phenyllithium.

SYNTHESIS AND RITTER REACTION OF 1,7,7-TRIMETHYL-2-PHENYLBICYCLOHEPTAN-2-EXO-OL

Kozlov, N. G.,Popova, L. A.,Vyalimyae, T. K.,Knizhnikov, V. A.,Ol'dekop, Yu. A.

, p. 702 - 705 (2007/10/02)

1,7,7-Trimethyl-2-phenylbicycloheptan-2-exo-ol is formed stereospecifically in the reaction of camphor with phenyllithium.The corresponding individual 1,7,7-trimethyl-4-phenylbicyclohept-2-yl-exo-acyl-amines were obtained as a result of the nucleophilic addition of acetonitrile, propionitrile, or methoxypropionitrile to this tertiary alcohol, which takes place in the presence of concentrated sulfuric acid.A scheme is proposed for their formation as a result of rearrangements of the intermediately formed 1,7,7-trimethylbicyclohept-2-yl cation.

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