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"2H-Pyran, tetrahydro-2-[[10-(phenylmethoxy)-7-undecynyl]oxy]-, (10R)-" is a complex organic compound belonging to the pyran family, characterized by a six-membered oxygen-containing ring. This specific compound features a tetrahydro structure, meaning it has four hydrogen atoms attached to the carbon backbone. The molecule contains a 10-(phenylmethoxy)-7-undecynyl group, which is a long-chain alkyne with a phenylmethoxy substituent at the 10th carbon. The "(10R)-" notation indicates that the compound has a specific stereochemistry at the 10th carbon, with the hydroxyl group oriented in the R configuration. 2H-Pyran, tetrahydro-2-[[10-(phenylmethoxy)-7-undecynyl]oxy]-, (10R)- is likely to be found in the realm of pharmaceuticals or as a synthetic intermediate due to its intricate structure and functional groups.

112775-35-6

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112775-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112775-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,7,7 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112775-35:
(8*1)+(7*1)+(6*2)+(5*7)+(4*7)+(3*5)+(2*3)+(1*5)=116
116 % 10 = 6
So 112775-35-6 is a valid CAS Registry Number.

112775-35-6Relevant academic research and scientific papers

STEREOCONTROLLED TOTAL SYNTHESIS OF THE MACROCYCLIC LACTONE (-)-ASPICILIN

Waanders, P.P.,Thijs, L.,Zwanenburg, B.

, p. 2409 - 2412 (2007/10/02)

The essential features of the enantiocontrolled total synthesis of (-)-aspicilin are the strategic use of the photochemical rearrangement of α,β-epoxy diazomethyl ketones to 4-hydroxyalkenoates (Scheme 1) and the stereochemical control of the Sharpless epoxidation, α,ο functionalization of an alkynol using potassium 3-aminopropylamine (KAPA) as acetylene zipper, coupling between C7 and C8 by means of a Wittig reaction and lactonization by using 2,6-dichlorobenzoyl chloride.

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