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6-methoxy-2-[3-phenylpropynoyl]phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1322774-91-3

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1322774-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1322774-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,7,7 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1322774-91:
(9*1)+(8*3)+(7*2)+(6*2)+(5*7)+(4*7)+(3*4)+(2*9)+(1*1)=153
153 % 10 = 3
So 1322774-91-3 is a valid CAS Registry Number.

1322774-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methoxy-2-[3-phenylpropynoyl]phenol

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:1322774-91-3 SDS

1322774-91-3Relevant academic research and scientific papers

Synthesis of γ-benzopyranone by TfOH-promoted regioselective cyclization of o-alkynoylphenols

Yoshida, Masahito,Fujino, Yuta,Doi, Takayuki

, p. 4526 - 4529 (2011/10/09)

Regioselective cyclization of o-alkynoylphenols forming γ-benzopyranones has been demonstrated. Trifluoromethanesulfonic acid (TfOH) induced 6-endo cyclization of o-alkynoylphenols without forming 5-exo cyclized benzofuranone derivatives to provide the corresponding γ-benzopyranones in high yields.

Regioselective synthesis of flavone derivatives via DMAP-catalyzed cyclization of o-alkynoylphenols

Yoshida, Masahito,Fujino, Yuta,Saito, Koya,Doi, Takayuki

, p. 9993 - 9997 (2012/02/06)

A catalytic amount of DMAP promoted cyclization of o-alkynoylphenols via a 6-endo cyclization mode leading to flavone derivatives in high yields without forming 5-exo cyclized aurone derivatives. Utilizing this method, methoxy substituted flavone and alkyl substituted γ-benzopyranone derivatives were synthesized.

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