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Furan, 2,3-dihydro-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56718-06-0

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56718-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56718-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56718-06:
(7*5)+(6*6)+(5*7)+(4*1)+(3*8)+(2*0)+(1*6)=140
140 % 10 = 0
So 56718-06-0 is a valid CAS Registry Number.

56718-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-2,3-dihydrofuran

1.2 Other means of identification

Product number -
Other names Furan,2,3-dihydro-3-phenyl

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:56718-06-0 SDS

56718-06-0Downstream Products

56718-06-0Relevant academic research and scientific papers

Rhodium-Catalyzed Diverse Arylation of 2,5-Dihydrofuran: Controllable Divergent Synthesis via Four Pathways

Dou, Xiaowei,Hayashi, Tamio,Lu, Tao,Xing, Junhao,Ye, Bihai,Zhu, Wanjiang

, p. 2958 - 2963 (2020/03/23)

The rhodium-catalyzed controllable diverse arylation of 2,5-dihydrofuran with arylboronic acids is reported. By fine-tuning of the reaction conditions, four different ring-opening or oxidative arylation pathways are controlled in the rhodium-catalyzed ary

Carbene reactions of α-oxacyclo- and α-azacyclo-N-aziridinylimines: Effect of heteroatom and ring size in the ring expansion reaction

Kim,Yoon

, p. 1622 - 1630 (2007/10/03)

Carbenes, generated from thermolysis of α-oxacyclo- and α-azacyclo-N-aziridinylimines in refluxing toluene, underwent ring expansions via insertion of alkyl carbenes into carbon-carbon bonds and intramolecular ammonium ylide formations, respectively. Ring expansion reaction of α-oxetanyl-N-aziridinylimines occurred via alkylidenecarbene intermediates, whereas thermal reaction of α-azetidinyl-N-aziridinylimines afforded α-aminoacetylene compounds via 1,2-H migration of alkylidenecarbene intermediates.

Generation and reaction of carbenes from α-oxacyclo-N-aziridinyl imines - A new method for ring expansion of cyclic ethers

Kim, Sunggak,Yoon, Joo-Yong,Cho, Chang Mook

, p. 909 - 910 (2007/10/03)

α-Oxetanyl-N-aziridinyl imines undergo ring expansion on heating to afford dihydrofurans via alkylidenecarbenes, whereas heating α-tetrahydrofuranyl and α-tetrahydropyranyl N-aziridinyl imines affords the ring expanded cyclic enol ethers via alkyl carbene

PALLADIUM-CATALYZED INTERMOLECULAR ALLYLIC ARYLATION OF CYCLOALKENES

Larock, Richard C.,Baker, Bruce E.

, p. 905 - 908 (2007/10/02)

Aryl halides and cycloalkenes undergo palladium-catalyzed, intermolecular, allylic cross-coupling in excellent yields under exceptionally mild reaction conditions.

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