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METHYL 4-ACETOXYCUBANECARBOXYLATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

225115-48-0

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225115-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225115-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,1,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 225115-48:
(8*2)+(7*2)+(6*5)+(5*1)+(4*1)+(3*5)+(2*4)+(1*8)=100
100 % 10 = 0
So 225115-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O4/c1-3(13)16-12-7-4-8(12)6-9(12)5(7)11(4,6)10(14)15-2/h4-9H,1-2H3

225115-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-acetyloxycubane-1-carboxylate

1.2 Other means of identification

Product number -
Other names BM551

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:225115-48-0 SDS

225115-48-0Downstream Products

225115-48-0Relevant academic research and scientific papers

Cubane Electrochemistry: Direct Conversion of Cubane Carboxylic Acids to Alkoxy Cubanes Using the Hofer–Moest Reaction under Flow Conditions

Collin, Diego E.,Folgueiras-Amador, Ana A.,Pletcher, Derek,Light, Mark E.,Linclau, Bruno,Brown, Richard C. D.

supporting information, p. 374 - 378 (2019/11/19)

The highly strained cubane system is of great interest as a scaffold and rigid linker in both pharmaceutical and materials chemistry. The first electrochemical functionalisation of cubane by oxidative decarboxylative ether formation (Hofer–Moest reaction) was demonstrated. The mild conditions are compatible with the presence of other oxidisable functional groups, and the use of flow electrochemical conditions allows straightforward upscaling.

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