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Furan, 2,5-dihydro-3-methyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56790-81-9

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56790-81-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56790-81-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,7,9 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56790-81:
(7*5)+(6*6)+(5*7)+(4*9)+(3*0)+(2*8)+(1*1)=159
159 % 10 = 9
So 56790-81-9 is a valid CAS Registry Number.

56790-81-9SDS

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-methyl-2-phenyl-2,5-dihydrofuran

1.2 Other means of identification

Product number -
Other names 2,5-dihydro-3-methyl-2-phenylfuran

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:56790-81-9 SDS

56790-81-9Downstream Products

56790-81-9Relevant academic research and scientific papers

Chemo-Enzymatic Metathesis/Aromatization Cascades for the Synthesis of Furans: Disclosing the Aromatizing Activity of Laccase/TEMPO in Oxygen-Containing Heterocycles

Risi, Caterina,Zhao, Fei,Castagnolo, Daniele

, p. 7264 - 7269 (2019/10/02)

The unprecedented Trametes versicolor laccase/TEMPO-catalyzed aromatization of 2,5-dihydrofurans to furans is described. A variety of furan derivatives have been synthesized in moderate to high conversions (21-99%) and yields (20-76%) under mild reaction

Chiral silver phosphate-catalyzed cycloisomeric kinetic resolution of α-allenic alcohols

Wang, Yan,Zheng, Kuan,Hong, Ran

supporting information; experimental part, p. 4096 - 4099 (2012/04/10)

A kinetic resolution of α-allenic alcohols is realized through chiral silver phosphate-catalyzed cycloisomerization with high stereoselectivity (selectivity factor up to 189) and tolerance of a variety of functional groups. A mechanistic model is proposed to interpret the origin of the high stereoselectivity and broad substrate scope.

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