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89263-93-4

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89263-93-4 Usage

Molecular weight

322.32 g/mol

Appearance

Colorless to white crystalline solid

Solubility

Soluble in organic solvents like ethanol, acetone, and diethyl ether; slightly soluble in water

Melting point

88-92°C

Boiling point

435-440°C

Density

1.25 g/cm3

Uses

a. Insecticide and acaricide for controlling pests on plants and crops
b. Treatment for scabies and lice infestations in humans and animals
c. Fragrance ingredient in perfumes
d. Flavoring agent in food and beverages
e. Studied for potential anti-inflammatory and anti-cancer properties

Safety precautions

Can be irritating to skin, eyes, and respiratory system; handle with care and use appropriate protective measures.

Check Digit Verification of cas no

The CAS Registry Mumber 89263-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,6 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89263-93:
(7*8)+(6*9)+(5*2)+(4*6)+(3*3)+(2*9)+(1*3)=174
174 % 10 = 4
So 89263-93-4 is a valid CAS Registry Number.

89263-93-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-hydroxy-3-(3-oxo-3-phenylpropanoyl)phenyl] benzoate

1.2 Other means of identification

Product number -
Other names 1,3-Propanedione,1-[5-(benzoyloxy)-2-hydroxyphenyl]-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:89263-93-4 SDS

89263-93-4Downstream Products

89263-93-4Relevant articles and documents

An Efficient One-Pot Synthesis and Anticancer Activity of 4'-Substituted Flavonoids

Wang,Liu,Zhang

, p. 1036 - 1041 (2018/07/06)

A number of 4'-substituted (R = H, Me, Cl, F) flavone derivatives is synthesized from 2-hydroxyacetophenones using the modified Baker–Venkataraman reaction. Compound [3-(4-fluorobenzoyl)-5- hydroxy-4'-fluoroflavone] was synthesized for the first time with the yield of 12%. Antiproliferative assays indicate that the synthesized flavones with F substituent at the 4' position demonstrate higher activity than the other flavone derivatives, particularly against HeLa and MCF-7 with the IC50 9.5 and 2.7 μM, respectively.

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