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17572-85-9

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17572-85-9 Usage

General Description

2,6-Diacetoxybicyclo[3,3,0]octane is a chemical compound with the molecular formula C12H18O4. It is a bicyclic organic compound, containing two acetate groups attached to a bicyclo[3,3,0]octane skeleton. 2,6-Diacetoxybicyclo[3,3,0]octane is often used in organic synthesis as a chiral building block, due to its rigid and symmetric structure. It can participate in various reactions such as Diels-Alder cycloadditions, forming complex organic molecules with high efficiency. Additionally, 2,6-Diacetoxybicyclo[3,3,0]octane has potential applications in the pharmaceutical industry, as it can be utilized in the synthesis of biologically active compounds. Overall, this compound plays a crucial role in the development of new molecules with diverse uses in chemistry and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 17572-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,7 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17572-85:
(7*1)+(6*7)+(5*5)+(4*7)+(3*2)+(2*8)+(1*5)=129
129 % 10 = 9
So 17572-85-9 is a valid CAS Registry Number.

17572-85-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-acetyloxy-1,2,3,3a,4,5,6,6a-octahydropentalen-1-yl) acetate

1.2 Other means of identification

Product number -
Other names rac-2-endo,6-endo-diacetoxy-cis-bicyclo<3.3.0>octane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17572-85-9 SDS

17572-85-9Downstream Products

17572-85-9Relevant articles and documents

Total Synthesis of (?)-Pepluanol B: Conformational Control of the Eight-Membered-Ring System

Chen, Peiqi,Fang, Ran,Li, Huilin,Liu, Meng,She, Xuegong,Wu, Chuanhua,Xie, Xingang,Zhang, Jing,Zhao, Gaoyuan,Zhou, Lin

supporting information, p. 3966 - 3970 (2020/02/05)

The first total synthesis of the Euphorbia diterpenoid pepluanol B in both racemic and enantioenriched form involves 20 steps from a known bicyclic diol. This synthesis features an unprecedented bromo-epoxidation to control the eight-membered-ring conform

NOVEL TRICYCLIC COMPOUNDS AS INHIBITORS OF MUTANT IDH ENZYMES

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Page/Page column 61-62, (2016/06/28)

The present invention is directed to tricyclic compounds of formula (I) which are inhibitors of one or more mutant IDH enzymes: (I); wherein A is -C(R1)= or -N=; and X is selected from the group consisting of: (II-i), (II-ii), (II-iii), and (II-iv). The present invention is also directed to uses of the tricyclic compounds described herein in the potential treatment or prevention of cancers in which one or more mutant IDH enzymes are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such cancers.

Total synthesis and NMR investigations of cylindramide

Cramer, Nicolai,Buchweitz, Maria,Laschat, Sabine,Frey, Wolfgang,Baro, Angelika,Mathieu, Daniel,Richter, Christian,Schwalbe, Harald

, p. 2488 - 2503 (2008/02/03)

Cylindramide (1) was built up from three components: a hydroxyornithine derivative 7, a tetrazolylsulfone 8, and a substituted pentalene subunit 9. Derivative 7 was prepared in a six-step reaction sequence involving the Wittig reaction and a Sharpless asy

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