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(1S,5R)-5-isopropyl-2-methylene cyclohexanol is a chiral organic compound characterized by its unique molecular structure. It features a cyclohexane ring with a methylidene group (CH2) at the 2-position, an isopropyl group at the 5-position, and a hydroxyl group at the 1-position. The compound's stereochemistry is defined by the (1S,5R) configuration, indicating that the hydroxyl group is on the same side of the molecule as the isopropyl group when viewed from the perspective of the cyclohexane ring. This specific arrangement of functional groups and stereochemistry is crucial for its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, where the three-dimensional structure of molecules can significantly influence their biological activity and reactivity.

7070-05-5

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7070-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7070-05-5 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 7070-05:
(6*7)+(5*0)+(4*7)+(3*0)+(2*0)+(1*5)=75
75 % 10 = 5
So 7070-05-5 is a valid CAS Registry Number.

7070-05-5Relevant academic research and scientific papers

FRAGRANCES WITH NOTE OF LILY OF THE VALLEY

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Paragraph 0274; 0275; 0276, (2013/04/13)

A compound of formula (I) is described and use thereof as fragrance, especially as lily-of-the-valley fragrance and/or as an agent for increasing the substantivity and/or the retention of a fragrance preparation and/or as a fixative.

Synthesis of the Alleged Natural Monoterpenoid α-Santolinenone

Guella, Graziano,Cavazza, Marino,Guerriero, Antonio,Pietra, Francesco

, p. 1248 - 1253 (2007/10/02)

Authentic α-santolinenone ( = (+)-(4R)-1(7)-p-menthen-2-one; (+)-1) is made available for the first time in 30 percent overall yield from (+)-(4R)-p-menthene ((+)-2) via the diastereomeric allylic alcohols (+)-4a/(+)-4b, which are oxidized to (+)-1 with Ag2CO3/Celite.Yields are good, except for the last stage; indeed, only alcohol (+)-4a, with equatorial OH-group, undergoes oxidation, and (+)-1 is partly substracted via a hetero Diels-Alder dimerization giving a mixture of the diastereomeric dihydropyrans (+)-5a/(+)-5b.When Cr(VI) reagents are used, (+)-4a/(+)-4b mainly give phelandral (6) and carvotanacetone (7).MnO2 reacts too sluggishly with (+)-4a/(+)-4b.A camphor pyrolyzate, previously thought to be 1 must be a different compound, probably 7.

Stereoselective Synthesis of Alcohols, IV Conformational Factors Determining the Stereochemistry of the Allyl Sulfoxide/ Allyl Sulfenate-Rearrangement

Hoffmann, Reinhard W.,Gerlach, Rainer,Goldmann, Siegfried

, p. 856 - 863 (2007/10/02)

The stereochemistry of the sigmatropic rearrangement of the conformationally rigid allyl sulfoxides 5 revealed a 6.2 fold preference for axial formation of the new C-O-bond.This preference dominates the 3.1 fold preference for an exo-versus endo-tran

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