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1,3-Dioxaspiro[4.4]nonan-6-ol,2,2,4-trimethyl-7-methylene-,(4R,5S,6R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

677752-15-7

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677752-15-7 Usage

Molecular structure

A complex and specific molecular structure with a spiro ring and two oxygen atoms.

Classification

Dioxaspiro compound.

Functional groups

Contains a methyl group and a methylene group.

Stereochemistry

Defined by the (4R,5S,6R) configuration, indicating the spatial arrangement of its substituent groups.

Applications

Potential uses in organic synthesis, pharmaceuticals, and industrial processes.

Research interest

Precise molecular structure makes it a subject of interest for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 677752-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,5 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 677752-15:
(8*6)+(7*7)+(6*7)+(5*7)+(4*5)+(3*2)+(2*1)+(1*5)=207
207 % 10 = 7
So 677752-15-7 is a valid CAS Registry Number.

677752-15-7Relevant academic research and scientific papers

Synthesis and structure of diastereomers of pentenocin B produced by Trichoderma hamatum FO-6903

Ohira, Susumu,Fujiwara, Hiroyuki,Maeda, Kiyomi,Habara, Masaharu,Sakaedani, Naomi,Akiyama, Megumi,Kuboki, Atsuhito

, p. 1639 - 1641 (2004)

All diastereomers of pentenocin B, an inhibitor of interleukin-1β converting enzyme produced by Trichoderma hamatum FO-6903, were synthesized in chiral forms starting from L-threonine. Absolute configurations of natural pentenocin B were clarified to be 4S, 5R, and 6R.

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