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2,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73522-43-7

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73522-43-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73522-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,5,2 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73522-43:
(7*7)+(6*3)+(5*5)+(4*2)+(3*2)+(2*4)+(1*3)=117
117 % 10 = 7
So 73522-43-7 is a valid CAS Registry Number.

73522-43-7Downstream Products

73522-43-7Relevant academic research and scientific papers

Co(II) catalysed oxidation of α-pinene by molecular oxygen. Part 2

Lajunen, Marja K.,Maunula, Tatja,Koskinen, Ari M.P.

, p. 8167 - 8171 (2000)

This paper reports studies of factors affecting air oxidation of (-)-α-pinene catalysed by Co(II)-pyridine complexes without a concomitant co-oxidant. Observations are presented about the nature and amount of the catalyst, reaction temperature, oxygen flow and solvent vs. non-solvent conditions. In addition, attention has been paid to the influence of added base or acid, and identification of side products. (C) 2000 Elsevier Science Ltd.

Photocatalytic Enantiodiscriminating Oxygenation with Cyclodextrin-linked Porphyrins and Molecular Oxygen

Weber, Lutz,Imiolczyk, Ines,Haufe, Guenter,Rehorek, Detlef,Hennig, Horst

, p. 301 - 303 (2007/10/02)

2,6-Permethylated β-cyclodextrin-linked iron and manganese porphyrins catalyse the enantioselective oxygenation of racemic mixture of (S)-α-pinene and (R)-α-pinene with molecular oxygen under irradiation with visible light.

Microbial Allyl Rearrangement and Resolution of Acetates of Unsaturated Cyclic Terpene Alcohols by Pseudomonas sp. NOF-5 Strain

Inagaki, Takashi,Ueda, Hiroo

, p. 2635 - 2640 (2007/10/02)

Microbial hydrolysis of the acetates of unsaturated cyclic terpene alcohols by Pseudomonas sp.NOF-5 isolated from soil was investigated. (+/-)-trans-Carveyl acetate ((+/-)-trans-3) was enantioselectively hydrolyzed with NOF-5 strain to give (-)-trans-carveol ((-)-trans-2 of 86.6percent optical purity).However, the hydrolysis of (+/-)-cis-3 was less enantioselective, while (+/-)-piperitylacetate ((+/-)-6, a cis and trans mixture) was hydrolyzed to give the (-)-trans- and (-)-cis-piperitols ((-)-trans-5 and (-)-cis-5) in a poor optical yield.In this case, other tert-alcohols, (+)-trans- and (-)-cis-2-p-menthen-1-ols ((+/-)-trans-7 and (-)-cis-7, were also produced.Furthermore, microbial and enzymic allyl rearrangements of (+)-trans-6 and (-)-trans-verbenylacetate ((-)-trans-11) were studied.Biological treatment of (+)-trans-6 and (-)-trans-11 with NOF-5 or its esterase gave (+)-trans- and (-)-cis-7 and (+)-cis-3-pinen-2-ol ((+)-cis-12), respectively.

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