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3-Buten-2-one, 1,1-dimethoxy-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55980-64-8

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55980-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55980-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,8 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55980-64:
(7*5)+(6*5)+(5*9)+(4*8)+(3*0)+(2*6)+(1*4)=158
158 % 10 = 8
So 55980-64-8 is a valid CAS Registry Number.

55980-64-8SDS

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 1,1-dimethoxy-4-phenylbut-3-en-2-one

1.2 Other means of identification

Product number -
Other names 1,1-dimethoxy-4-phenyl-3-buten-2-one

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:55980-64-8 SDS

55980-64-8Relevant academic research and scientific papers

Synthesis of a series of aldol compounds by direct LDA reaction from pyruvaldehyde dimethyl acetal and 3-arylmethylidine pentane-2,4-diones by Knoevenagel reaction

Chakraborty, Shampa,Goswami, Shyamaprosad,Quah, Ching Kheng

, p. 623 - 627 (2020/07/02)

A new convenient synthesis of aldol compounds starting from pyruvaldehyde dimethyl acetal has been described. This method conveniently led to the synthesis of some biologically important compounds1,2. A new synthesis of 3-arylmethylidine pentan

Selenium-Catalyzed Conversion of Methyl Ketones into α-Keto Acetals

Tiecco, M.,Testaferri, L.,Tingoli, M.,Bartoli, D.

, p. 4523 - 4528 (2007/10/02)

The reaction of methyl ketones with catalytic amounts of diphenyl diselenide and an excess of ammonium peroxydisulfate in methanol proceeds smoothly to afford α-keto acetals in good yield.In some cases reaction yields were increased by using stoichiometri

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