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Ethanone, 1-(5-benzoyl-2-methyl-3-furanyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61667-75-2

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61667-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61667-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61667-75:
(7*6)+(6*1)+(5*6)+(4*6)+(3*7)+(2*7)+(1*5)=142
142 % 10 = 2
So 61667-75-2 is a valid CAS Registry Number.

61667-75-2SDS

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 1-(5-benzoyl-2-methylfuran-3-yl)ethanone

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:61667-75-2 SDS

61667-75-2Downstream Products

61667-75-2Relevant academic research and scientific papers

Preparation of 4-(Nitromethyl)furan Derivatives and Their Application in the Syntheses of Bis(furan-2-yl)oximes

Wan, Yinbo,Zhu, Yang,Peng, Haiyun,Deng, Guisheng

, p. 281 - 293 (2021/12/27)

An efficient method for the preparation of tetrasubstituted furans, which contains a nitromethyl group at the 4-position, has been developed. The applications of 4-(nitromethyl)furans on the synthesis of highly functionalized bis(furyl)oxime were explored

AgOTf/I2-Mediated Cyclization/Cross-Coupling/Isomerization of Enynones with Phosphorus Ylides: An Expedient Route to Stereoselective Synthesis of (E)-2-Alkenylfurans

Deng, Guisheng,Tang, Ling,Zhang, Yangyi

, p. 13245 - 13251 (2021/10/01)

Ag(I)-catalyzed cascade reactions involving enynone cyclization and cross-coupling with phosphorus ylides have been achieved for the first time. Subsequent treatment of the reaction mixture with I2 afforded the corresponding (E)-α-alkenylfurans in 73-95%

An efficient nanoparticle-supported and magnetically recoverable copper(I) catalyst for synthesis of furans from ene-yne-ketone

Liu, Yi,Liu, Zhan,Cui, Yingde

supporting information, p. 175 - 180 (2015/03/04)

A magnetic nano-supported Cu(I) catalyst was prepared and showed high activity for cyclization of ene-yneketone to synthesize furans. The catalyst was easily recovered from the reaction by using external magnets and reused 8 times without significant loss

Palladium-catalyzed formation of C=C bonds: A regioselective strategy for the synthesis of 2-vinylfurans by 1,2-H shift of palladium-carbene complexes

Zhan, Haiying,Lin, Xiulian,Qiu, Yanying,Du, Zuodong,Li, Peixian,Li, Yongjian,Cao, Hua

, p. 2284 - 2287 (2013/05/22)

A convenient method to synthesize vinylfurans through a palladium-catalyzed cyclization/1,2-H shift sequence under mild conditions is described. This is an efficient strategy to synthesize 2-vinylfurans from ene-yne ketones, and the corresponding products

Copper-catalyzed C-O bond formation: An efficient one-pot highly regioselective synthesis of furans from (2-furyl)carbene complexes

Cao, Hua,Zhan, Haiying,Cen, Jinghe,Lin, Jingxin,Lin, Yuanguang,Zhu, Qiuxia,Fu, Minling,Jiang, Huanfeng

, p. 1080 - 1083 (2013/03/29)

A convenient one-pot Cu(I)-catalyzed strategy for regioselective synthesis of trisubstituted furan derivatives has been developed via (2-furyl) carbene complexes. This process has opened a new synthetic route to a variety of α-carbonyl furans using air as

Synthesis of 2-acylfurans from 3-(1-alkynyl)-2-alken-1-ones via the oxidation of gold-carbene intermediates by H2O2

Wang, Tao,Zhang, Junliang

, p. 4270 - 4273 (2010/07/04)

An efficient approach to 2,4,5-trisubstituted 2-acylfurans is described: treating 3-(1-alkynyl)-2-alken-1-ones with AuCl3 in DCM at rt in the presence of H2O2 afforded good yields of 2-acylfurans.

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