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2,5-anhydro-1,6-di-O-benzoyl-3,4-dideoxy-D-threo-hex-3-enitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91422-50-3

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91422-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91422-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91422-50:
(7*9)+(6*1)+(5*4)+(4*2)+(3*2)+(2*5)+(1*0)=113
113 % 10 = 3
So 91422-50-3 is a valid CAS Registry Number.

91422-50-3Relevant academic research and scientific papers

Chiral Pool/Henry/Enzymatic routes to acetogenin synthons

Qayed, Wesam S.,Luzzio, Frederick A.

, p. 622 - 630 (2015/11/09)

Enantio specific and enantioselective approaches to the natural (16 R,19R)- and the unnatural (16S,19S)- THF core of the bioactive acetogenin annonacin are described which utilizes both a chiral pool synthesis and enzymatic transformations. In the antipodal (2S,5S) THF series derived from D-(+)-glucosamine, the semi-protected THF aldehyde synthon allows for two-directional synthetic elaboration through a Henry reaction with a lipid-like nitroalkane. The resulting nitroalcohol having the unnatural (2S,5S)-THF core was oxidized to the corresponding a-nitroketone using a modified Collins oxidation. The intermediate a-nitroketone has potential for the preparation of the C15-C32 core and analogues through subsequent removal of the nitro group and reduction of the carbonyl.

2,5-ANHYDRO-D-HEXITOLS: SYNTHESES OF 2,5-ANHYDRO-D-ALTRITOL AND 2,5-ANHYDRO-D-IDITOL

Otero, Dario A.,Simpson, Ronald

, p. 79 - 86 (2007/10/02)

2,5-Anhydro-D-altritol (2a) and the previously-unknown 2,5-anhydro-D-iditol (3a) have been prepared from 2,5-anhydro-D-mannitol (1a).The preparation of 3a from the intermediate epoxide 7b is particularly sensitive to pH, and a mechanism is proposed to explain this.Attention is drawn to the limitations of the trifluoroperacetic acid-disodium hydrogenphosphate procedure for the epoxidation of alkenes of diminished reactivity.

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