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136796-00-4

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136796-00-4 Usage

Origin

Derivative of ferulic acid, a natural phenolic compound found in plant cell walls

Potential Pharmaceutical Applications

Studied for potential therapeutic effects on human health

Beneficial Effects

Antioxidant, anti-inflammatory, and anti-cancer properties

Research Areas

Neurodegenerative diseases
Cardiovascular diseases
Diabetes

Mechanism of Action

Inhibits the enzyme ferulic acid decarboxylase

Research Focus

Inhibition of harmful compound production in the human body

Promising Potential

Various therapeutic applications
Need for Further Research and Development

Check Digit Verification of cas no

The CAS Registry Mumber 136796-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,9 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136796-00:
(8*1)+(7*3)+(6*6)+(5*7)+(4*9)+(3*6)+(2*0)+(1*0)=154
154 % 10 = 4
So 136796-00-4 is a valid CAS Registry Number.

136796-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-acetyl-2-hydroxyphenyl)-3-methoxybutan-2-one

1.2 Other means of identification

Product number -
Other names 3-(4-acetyl-2-hydroxy-phenyl)-3-methoxy-butan-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:136796-00-4 SDS

136796-00-4Downstream Products

136796-00-4Relevant articles and documents

Epoxidation of 2,3-Dimethylbenzofurans by Dimethyldioxirane

Adam, Waldemar,Bialas, Joachim,Hadjiarapoglou, Lazaros,Sauter, Markus

, p. 231 - 234 (2007/10/02)

The synthesis of epoxides 2 by the reaction of the chloro- and methyl-substituted 2,3-dimethylbenzofuranes 1 with dimethyldioxirane at low temperature is reported.These labile epoxides were spectroscopically characterized (1H and 13C NMR) at subambient temperatures.Epoxidation of benzofuran 1c affords a 31:69 mixture of epoxide 2c and quinone methide 3c, the latter presumably being produced by valence isomerization of the epoxide.On warming up above -10 deg C, the epoxides 2 suffer decomposition.Treatment of epoxide 2i with methanol yields the tautomeric mixture ofadducts 4i and 4i'.Key Words: Epoxidation / Dioxirane, dimethyl / Benzofurans, 2,3-dimethyl- / Benzofuran epoxides / Quinone methides / Methanol addition

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