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Methanone, (2,5-dimethoxyphenyl)(2-hydroxy-4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62495-96-9

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62495-96-9 Usage

Preparation

Preparation by reaction of 2,5-dimethoxy benzoic acid with 3-methoxyphenol in the presence of zinc chloride and phosphorous oxychloride at 65–70° for 2 h (21%).

Check Digit Verification of cas no

The CAS Registry Mumber 62495-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62495-96:
(7*6)+(6*2)+(5*4)+(4*9)+(3*5)+(2*9)+(1*6)=149
149 % 10 = 9
So 62495-96-9 is a valid CAS Registry Number.

62495-96-9SDS

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 (2,5-dimethoxyphenyl)-(2-hydroxy-4-methoxyphenyl)methanone

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-2',4,5'-trimethoxybenzophenon

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:62495-96-9 SDS

62495-96-9Downstream Products

62495-96-9Relevant academic research and scientific papers

γ-Pyrone compounds. IV: Synthesis and antiplatelet effects of mono- and dioxygenated xanthones and xanthonoxypropanolamine

Lin,Liou,Ko,Teng

, p. 11 - 16 (2007/10/02)

Xanthodilol, mono- and dioxygenated xanthones, and 1,3-, 2,3-, 3,4-, 3,5- , 1,6-, 2,6-, and 3,6-dioxygenated xanthones were synthesized from benzophenone precursors by Friedel-Crafts acylation and subsequent base- catalyzed cyclization to eliminate methanol. 3-Hydroxyxanthone, xanthodilol, 2,3-dihydroxyxanthone diacetate, and 3,4-dihydroxyxanthone and its diacetate showed potent antiplatelet effects on arachidonate- and collagen-induced aggregation. 3,5-Dihydroxyxanthone and its diacetate, 1,6-dimethoxyxanthone, and 3,6-dihydroxyxanthone and its diacetate showed potent antiplatelet effects on arachidonate-induced aggregation.

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