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Bicyclo[4.2.0]octa-1,3,5-trien-7-one, 3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126889-61-0

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126889-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126889-61-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,8 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 126889-61:
(8*1)+(7*2)+(6*6)+(5*8)+(4*8)+(3*9)+(2*6)+(1*1)=170
170 % 10 = 0
So 126889-61-0 is a valid CAS Registry Number.

126889-61-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbicyclo[4.2.0]octa-1(6),2,4-trien-7-one

1.2 Other means of identification

Product number -
Other names -

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:126889-61-0 SDS

126889-61-0Relevant academic research and scientific papers

Preparation of Benzocyclobutenones via the Photochemical Cyclization of 1-(ortho-Alkylary)-2,2,4-trimethylpentane-1,3-diones

Yoshioka, Michikazu,Momose, Shinobu,Nishizawa, Kaori,Hasegawa, Tadashi

, p. 499 - 503 (2007/10/02)

Irradiation of 1-(ortho-methylaryl)- and 1-(ortho-ethylaryl)-2,2,4-trimethylpentane-1,3-diones 4a-g in hexane gave benzocyclobutenols 10a-g.However, irradiation of 1-(ortho-isopropylaryl)-2,2,4-trimethylpentane-1,3-diones 4i and 4j resulted in no reaction.Irradiation of 1-mesityl-2,2,4-trimethylpentane-1,3-dione 4h gave a complex mixture of products.Pyrolysis of benzocyclobutenols 10a, b, d-f gave benzocyclobutenones 11a, b, d-f and 2,4-dimethylpentan-3-one 2, whereas that of the benzocyclobutenols 10c, g gave the starting 1,3-diketones 4c, g predominantly along with small amounts of benzocyclobutenones 11c, g and the dimethylpentanone 2.

THERMAL ADDITION REACTIONS TO BENZOCYCLOBUTENONES STUDIED BY FLASH PHOTOLYSIS

Schiess, P.,Eberle, M.,Huys-Francotte, M.,Wirz, J.

, p. 2201 - 2204 (2007/10/02)

Ortho-quinoid vinylketenes 2 have been generated thruogh flash photolysis of benzocyclobutenones 1.A kinetic study of intermolecular addition reactions of 2 competing with the recyclization 2 -> 1 reveals strikingly different substituent effects for the addition of methanol and of dienophiles.

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