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1H-INDEN-1-ONE, 6-METHOXY- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38480-95-4

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38480-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38480-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,8 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38480-95:
(7*3)+(6*8)+(5*4)+(4*8)+(3*0)+(2*9)+(1*5)=144
144 % 10 = 4
So 38480-95-4 is a valid CAS Registry Number.

38480-95-4SDS

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 6-methoxyinden-1-one

1.2 Other means of identification

Product number -
Other names 6-Methoxy-1-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:38480-95-4 SDS

38480-95-4Relevant academic research and scientific papers

Synthesis of benzo[c]fluorenone through a one-pot cascade reaction using inden-1-one derivatives

Zheng, Shuyan,Tan, Hongsheng,Zhang, Xiaoguang,Yu, Chunhui,Shen, Zhengwu

supporting information, p. 975 - 978 (2015/02/02)

A novel one-pot thermal cycloaddition of two indenones followed by a decarbonylation and dehydrogenation cascade afforded benzo[c]fluorenones regioselectively. Various substituted indenone derivatives were converted into their corresponding benzo[c]fluorenones in good to excellent yields.

Synthesis of benzo[c]fluorenone through a one-pot cascade reaction using inden-1-one derivatives

Zheng, Shuyan,Tan, Hongsheng,Zhang, Xiaoguang,Yu, Chunhui,Shen, Zhengwu

supporting information, p. 975 - 978 (2014/02/14)

A novel one-pot thermal cycloaddition of two indenones followed by a decarbonylation and dehydrogenation cascade afforded benzo[c]fluorenones regioselectively. Various substituted indenone derivatives were converted into their corresponding benzo[c]fluorenones in good to excellent yields.

Synthesis of enantiopure angularly condensed [2.2]paracyclophanes containing five-membered rings

Minuti, Lucio,Taticchi, Aldo,Marrocchi, Assunta,Lanari, Daniela,Broggi, Alessandra,Gacs-Baitz, Eszter

, p. 481 - 487 (2007/10/03)

Optically active angularly condensed [2.2]paracyclophanes containing five-membered rings have been synthesized by a two-step approach based on the Diels-Alder cycloaddition of (S)-(+)-4-vinyl[2.2]paracyclophane. Structural analysis by NMR spectroscopy is presented. These helicenophanes containing a cyclopentane ring show extraordinarily high specific rotations. This phenomenon has been discussed in terms of structural modifications caused by the replacement of the benzene unit with a cyclopentane ring.

Facile synthesis of indenones from indanones: A new procedure

Hauser,Zhou,Sun

, p. 77 - 80 (2007/10/03)

A two-step procedure for the conversion of indanones to indenones is described.

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