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112892-88-3

112892-88-3

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112892-88-3 Usage

General Description

4-Carboxaldehydebenzocyclobutene is a chemical compound with the molecular formula C9H6O2. It comes under the category of organic compounds known as benzocyclobutenes which are polycyclic aromatic compounds containing a benzene ring fused to a cyclobutene ring. This chemical compound’s systematic name is 4-formylcyclohexa-2,5-dienecarboxylic acid. Characteristics with regard to its physical properties, applications, toxicity, or potential uses in research or industry are not widely documented, indicating it may not be extensively investigated or commonly used.

Check Digit Verification of cas no

The CAS Registry Mumber 112892-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112892-88:
(8*1)+(7*1)+(6*2)+(5*8)+(4*9)+(3*2)+(2*8)+(1*8)=133
133 % 10 = 3
So 112892-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O/c10-6-7-1-2-8-3-4-9(8)5-7/h1-2,5-6H,3-4H2

112892-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[4.2.0]octa-1(6),2,4-triene-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-carbaldehydebenzocyclobutene

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:112892-88-3 SDS

112892-88-3Relevant articles and documents

A facile synthesis of bicyclo[4.2.0]octa-1,3,5-trien-3-ol

Thomas,Pews

, p. 2335 - 2340 (1991)

Bicyclo[4.2.0]octa-1,3,5-trien-3-ol (2) has been synthesized in good yield via a Baeyer-Villiger reaction of the corresponding aldehyde 5 with permonophosphoric acid.

First synthesis of optically active benzocyclobutene and biphenylene-based unusual α-amino acid derivatives

Kotha, Sambasivarao,Sreenivasachary, Nampally,Halder, Somnath

, p. 2565 - 2568 (1999)

Various optically pure benzocyclobutene and biphenylene-based α-amino acid derivatives are prepared in a very high diastereoselective manner via a six step sequence using Schollkopf chiral auxiliary.

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH NLRP ACTIVITY

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Page/Page column 286-287, (2020/06/05)

In one aspect, compounds of Formula AA, or a pharmaceutically acceptable salt thereof, are featured or a pharmaceutically acceptable salt thereof, wherein the variables shown in Formula A can be as defined anywhere herein.

FULLERENE DERIVATIVES

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Page/Page column 11, (2012/06/18)

A fullerene derivative having a partial structure represented by formula (1): wherein R represents a monovalent group, and r represents an integer of 0 to 4, in particular, a fullerene derivative, which has one to four structures represented by formula (1), can be applied to an organic photoelectric conversion element having a high open-circuit voltage and is therefore suitable for an organic thin-film solar cell or an organic photosensor, and thus it is extremely useful.

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