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(S)-(-)-p-mentha-1,8(10)-dien-9-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10067-33-1

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10067-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10067-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10067-33:
(7*1)+(6*0)+(5*0)+(4*6)+(3*7)+(2*3)+(1*3)=61
61 % 10 = 1
So 10067-33-1 is a valid CAS Registry Number.

10067-33-1Upstream product

10067-33-1Downstream Products

10067-33-1Relevant academic research and scientific papers

Stereoselective Synthesis of Limonene-Based Chiral 1,3-Amino Alcohols and Aminodiols

Le Minh, Tam,Fül?p, Ferenc,Szakonyi, Zsolt

, p. 6708 - 6713 (2017/12/07)

An unexpected ring-closing reaction of an α,β-unsaturated carboxylic acid, derived from (R)- and -(S)-limonene, in the presence of trifluoroacetic anhydride (TFAA) resulted in bicyclic α-methylene ketones and their hydroxylated analogues in a stereoselective intramolecular acylation reaction. The reaction was studied in detail, and was optimised for both compounds. The addition of secondary and primary amines to both keto alkenes followed by in-situ reduction of the resulting aminoketones with sodium borohydride gave new bicyclic terpenoid secondary and tertiary 1,3-amino alcohols and aminodiols with excellent diastereoselectivities. Regioisomeric aminodiols were prepared stereoselectively from the unsaturated 1,3-amino alcohols by hydroboration with Me2S·BH3/H2O2.

A chemoenzymatic, preparative synthesis of the isomeric forms of p-menth-1-en-9-ol: Application to the synthesis of the isomeric forms of the cooling agent 1-hydroxy-2,9-cineole

Serra, Stefano,Fuganti, Claudio,Gatti, Francesco G.

experimental part, p. 1031 - 1037 (2009/04/05)

A preparative-scale synthesis of the four p-menth-1-en-9-ol isomers 2a-5a has been achieved by means of two chemoenzymatic processes. Both synthetic pathways start from the enantiomeric forms of limonene that are converted into p-mentha-1,8-dien-9-al isomers 12 and 15. The baker's yeast mediated reduction of the latter aldehydes afforded compounds 3a and 5a, respectively, with very high enantioselectivity. Moreover, chemical reduction of 12 and 15 gives the mixtures of enantiopure diastereoisomers 2a/3a and 4a/5a, respectively. PPL (Porcine pancreas lipase) mediated resolution of the latter mixtures followed by fractionating crystallization of derivatives 2b-5b allowed the enantio- and diastereoisomerically pure alcohols 2a-5a to be obtained. Compounds 2a-5a have then been used as starting materials for the preparation of four isomers of the cooling agent 1-hydroxy-2,9-cineole (6-9). Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Asymmetric Total Synthesis of Pseudoplexaurol and 14-Deoxycrassin, two Antitumor Marine Cembrane Diterpenoids

Liu, Zuosheng,Peng, Lizeng,Li, Weidong Z.,Li, Yulin

, p. 1977 - 1980 (2007/10/03)

The first asymmetric total synthesis of two naturally occurring antitumor pseudoplexaurol and 14-deoxycrassin were achieved via two convergent synthetic sequences featured a chiral pool protocol to implement C-1 stereogenic center and Ti(0)-mediated cyclization leading to cembrane ring.

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