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4H-1-Benzopyran-4-one, 5,7-bis(benzoyloxy)-2,3-dihydro-3-[(4-methoxyphenyl)methylene]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54107-64-1

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54107-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54107-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,0 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54107-64:
(7*5)+(6*4)+(5*1)+(4*0)+(3*7)+(2*6)+(1*4)=101
101 % 10 = 1
So 54107-64-1 is a valid CAS Registry Number.

54107-64-1SDS

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 5,7-dibenzoyloxy-3-(4'-methoxybenzylidene)chroman-4-one

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:54107-64-1 SDS

54107-64-1Downstream Products

54107-64-1Relevant academic research and scientific papers

Chemistry of Homoisoflavonoids: Synthesis of Polyhydroxy 3-Benzylchromones and 3-Benzylchroman-4-ones without Protection and Deprotection of Hydroxyl Groups and a Convenient Preparation of Benzylidenechroman-4-ones

Sathyanarayana, S.,Krishnamurty, H. G.

, p. 899 - 901 (2007/10/02)

Catalytic transfer hydrogenation of hydroxyflavanones gives hydroxydihydrochalcones.These dihydrochalcones are converted into hydroxyhomoisoflavones and homoisoflavanones without protection and deprotection of hydroxyl groups.The condensation between chromanones and aryl aldehydes in the presence of dry p-toluenesulfonic acid in benzene or toluene gives benzylidenechromanones in good yields.The method is far superior to all other existing procedures.

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