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1H-Indene, 3-methoxy-1,2-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65684-96-0

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65684-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65684-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,8 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65684-96:
(7*6)+(6*5)+(5*6)+(4*8)+(3*4)+(2*9)+(1*6)=170
170 % 10 = 0
So 65684-96-0 is a valid CAS Registry Number.

65684-96-0SDS

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 3-Methoxy-1,2-diphenyl-1H-indene

1.2 Other means of identification

Product number -
Other names 1-methoxy-2,3-diphenylindene

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:65684-96-0 SDS

65684-96-0Downstream Products

65684-96-0Relevant academic research and scientific papers

Acidic Co-Catalysts in Cationic Gold Catalysis

Barrio, Pablo,Kumar, Manish,Lu, Zhichao,Han, Junbin,Xu, Bo,Hammond, Gerald B.

, p. 16410 - 16414 (2016/11/09)

A systematic study on the effects of Lewis or Br?nsted acid co-catalysts in gold-catalyzed reactions was undertaken using representative reactions (O-, N-, and C-nucleophilic additions to alkynes). Through these reactions, it was demonstrated that an acidic co-catalyst can increase the catalyst turnover significantly, enabling practical reaction rates at competitive catalyst loadings (1 mol %). Further investigation is currently underway to improve the understanding of the subtle principles underlying these experimental observations.

Synthesis of indenyl ethers by gold(I)-catalyzed intramolecular carboalkoxylation of alkynes

Dube, Pascal,Toste, F. Dean

, p. 12062 - 12063 (2007/10/03)

The gold(I)-catalyzed carboalkoxylation of alkynes to form indanone derivatives from readily available ortho-acetylenic benzylic ethers is described. Importantly, the gold(I)-catalyzed rearrangement of enantioenriched benzylic ethers proceeds with chirali

Generation and Trapping of Cyclopropenes from 2-Alkoxy-1,1-dichlorocyclopropanes

Mueller, Paul,Pautex, Nicole

, p. 55 - 64 (2007/10/02)

In presence of crown ether, 2-alkoxy-1,1-dichlorocyclopropanes react with t-BuOK/THF preferentially via ring opening to 2-chloroalk-2-en-1-ones and alkynones or to chlorocyclopropenes.The latter may be intercepted with 1,3-diphenylisobenzofuran, but in th

Solvent, chelation and concentration effects on the benzannulation reaction of chromium carbene complexes and acetylenes

Chan, Kin Shing,Peterson, Glen A.,Brandvold, Timothy A.,Faron, Katherine L.,Challener, Cynthia, A.,et al.

, p. 9 - 56 (2007/10/02)

The reactions of a number of chromium carbene complexes (CO)5Cr=C(OMe)R (R = Ph, o-OMePh, p-OMePh, o-O-tBuPh, 1-C6H9, 1-C5H7O) were examined with a variety of acetylenes (R'CCR2, R1, R2 = H, Me, Et, n-Pr, Ph, SiMe3) in sol

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