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1H-Inden-1-one, 3-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

705255-91-0

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705255-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 705255-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,2,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 705255-91:
(8*7)+(7*0)+(6*5)+(5*2)+(4*5)+(3*5)+(2*9)+(1*1)=150
150 % 10 = 0
So 705255-91-0 is a valid CAS Registry Number.

705255-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)inden-1-one

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenyl)indenone

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:705255-91-0 SDS

705255-91-0Downstream Products

705255-91-0Relevant academic research and scientific papers

Ir-catalyzed asymmetric hydrogenation of 3-arylindenones for the synthesis of chiral 3-arylindanones

Yan, Jun,Nie, Yu,Gao, Feng,Yuan, Qianjia,Xie, Fang,Zhang, Wanbin

supporting information, (2021/02/27)

An efficient synthesis of chiral 3-arylindanones via iridium-catalyzed asymmetric hydrogenation of 3-arylindenones has been developed. The reaction showed good compatibility with various functional groups, delivering a variety of 3-arylindanones in excellent yields and with good enantioselectivities. The reaction was also carried out on a gram-scale, delivering the product in quantitative yield. In addition, the products can be easily derivatized and transformed into natural products and pharmaceutical agents.

Stereoselective Photodimerization of 3-Arylindenones in Solution and in the Solid State

Uemura, Naohiro,Ishikawa, Hiroki,Tamura, Naoki,Yoshida, Yasushi,Mino, Takashi,Kasashima, Yoshio,Sakamoto, Masami

, p. 2256 - 2262 (2018/02/23)

Photodimerization of 3-arylindenones in solution and in the solid state was examined. Irradiation of 3-arylindenones in benzene exclusively gave C2-symmetric anti-HH cyclobutane dimers in good yields. In contrast, photolysis in the solid state

A facile approach to the construction of 1H-inden-1-one

Chen, Bo,Xie, Xingang,Lu, Jiangping,Wang, Qiaoling,Zhang, Jiyong,Tang, Shouchu,She, Xuegong,Pan, Xinfu

, p. 259 - 262 (2007/10/03)

The one-pot synthesis of 1H-inden-1-one from 1-(2-bromoaryl)prop-2-en-1-ol was described. The reaction involved a sequential intramolecular Heck reaction followed by an aerial oxidation of allylic alcohol. Georg Thieme Verlag Stuttgart.

Protonation and cyclization of 1,3-diarylpropynones in superacids

Vasil'ev,Walspurger,Pale,Sommer,Haouas,Rudenko

, p. 1769 - 1778 (2007/10/03)

1,3-Diarylpropynones ArC≡CCOAr′ in superacids with H 0 ranging from -20 to - 14 undergo protonation at the carbonyl oxygen atoms to give stable ArC≡CC(O+H)Ar′ ions or at the acetylenic C2 atom with formation of reactive Ar

Chemistry of 1,3-diarylpropynones in superacids

Vasilyev,Walspurger,Haouas,Sommer,Pale,Rudenko

, p. 3483 - 3489 (2007/10/03)

In superacids with H0 = -14 to -20, it has been found that 1,3-diarylpropynones ArC≡CCOAr′ are either protonated on oxygen of carbonyl groups with the formation of stable ions ArC≡CC(O +H)Ar′ or undergo further transformations when t

A new, fast and efficient synthesis of 3-aryl indenones: Intramolecular cyclization of 1,3-diarylpropynones in superacids

Vasilyev, Aleksander V.,Walspurger, Stéphane,Pale, Patrick,Sommer, Jean

, p. 3379 - 3381 (2007/10/03)

1,3-Diarylpropynones were cleanly converted to the corresponding 3-arylindenones in various superacidic media. This new, simple, one-pot reaction proved to be efficient (yields up to 95%) and very fast (reaction time less than 30min).

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