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Benzene, 1,4-dimethoxy-2-(2-propenyloxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

591249-40-0

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591249-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 591249-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,1,2,4 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 591249-40:
(8*5)+(7*9)+(6*1)+(5*2)+(4*4)+(3*9)+(2*4)+(1*0)=170
170 % 10 = 0
So 591249-40-0 is a valid CAS Registry Number.

591249-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(allyloxy)-1,4-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names 2-allyloxy-1,4-dimethoxybenzene

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:591249-40-0 SDS

591249-40-0Relevant academic research and scientific papers

Synthesis of coumarins by ring-closing metathesis using Grubbs' catalyst

Nguyen Van, Tuyen,Debenedetti, Silvia,De Kimpe, Norbert

, p. 4199 - 4201 (2003)

A novel generally applicable synthesis of coumarins from phenolic substrates utilizing ring-closing metathesis is described. This sequence involves O-allylation of phenols followed by ortho-Claisen rearrangement, subsequent based-induced isomerization affording 2-(1-propenyl)phenols, acylation with acryloyl chloride, and finally ring-closing metathesis (RCM) with Grubbs' second generation catalyst.

Synthetic models related to methoxalen - CYP2A6 interactions. Dimethoxybenzofuran derivatives as potent and selective inhibitors of cyp2a6

Yamaguchi, Yuki,Akimoto, Ichie,Motegi, Kyoko,Yoshimura, Teruki,Wada, Keiji,Nishizono, Naozumi,Oda, Kazuaki

, p. 1727 - 1739 (2013/09/12)

The human CYP2A6 enzyme metabolizes several xenobiotics including nicotine, the addictive component in tobacco. Reduced activity of CYP2A6, either for genetic reasons or by administering inhibitors of CYP2A6, reduces tobacco smoking. The reported compound

An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans

Van Otterlo, Willem A.L.,Morgans, Garreth L.,Madeley, Lee G.,Kuzvidza, Samuel,Moleele, Simon S.,Thornton, Natalie,De Koning, Charles B.

, p. 7746 - 7755 (2007/10/03)

Twelve substituted benzofurans were synthesized from their corresponding substituted 1-allyl-2-allyloxybenzenes using ruthenium-mediated C- and O-allyl isomerization followed by ring-closing metathesis.

Ring-closing metathesis for the synthesis of 2H- and 4H-chromenes

Van Otterlo, Willem A.L.,Ngidi, E. Lindani,Kuzvidza, Samuel,Morgans, Garreth L.,Moleele, Simon S.,De Koning, Charles B.

, p. 9996 - 10006 (2007/10/03)

Six 4H-chromenes were synthesized from substituted phenols using vinylstannylation and ring-closing metathesis (RCM) as key steps. In addition, a different approach involving amongst other steps, an aryl allyl isomerization and RCM afforded a set of seven 2H-chromenes from phenolic precursors.

Ring-closing metathesis for the synthesis of benzo-fused bicyclic compounds

Van Otterlo, Willem A.L.,Ngidi, E. Lindani,Coyanis, E. Mabel,De Koning, Charles B.

, p. 311 - 313 (2007/10/03)

Ring-closing metathesis (RCM) was used to synthesise five 4H-chromenes, a naphthol and an indenol. These are the first examples of RCM applied to the synthesis of such benzo-fused bicyclic compounds.

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