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107585-77-3

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107585-77-3 Usage

General Description

4'-Demethyl-3,9-dihydroeucomin is a chemical compound that falls into the class of organic compounds known as indolizidines. Indolizidines are polycyclic compounds that contain an indolizidine moiety, which is a bicyclic compound made up of a two-ring system containing a three-membered ring and a pyrrole, fused together. Information about the specific properties, uses, and potential hazards of 4'-Demethyl-3,9-dihydroeucomin is scarce; as it seems to be less common or less studied than some other chemical compounds. Its properties would be determined in part by its structure, so it's likely that it shares some characteristics common to indolizidines.

Check Digit Verification of cas no

The CAS Registry Mumber 107585-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,8 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107585-77:
(8*1)+(7*0)+(6*7)+(5*5)+(4*8)+(3*5)+(2*7)+(1*7)=143
143 % 10 = 3
So 107585-77-3 is a valid CAS Registry Number.

107585-77-3SDS

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 5,7-Dihydroxy-3-(4-hydroxybenzyl)-2,3-dihydro-4H-chromen-4-one

1.2 Other means of identification

Product number -
Other names 4'-demethyl-5-O-methyl-dihydroeucomin

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:107585-77-3 SDS

107585-77-3Downstream Products

107585-77-3Relevant articles and documents

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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