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2,5-Cyclohexadien-1-one, 3,4,4-trimethoxy-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72796-36-2

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72796-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72796-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,9 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72796-36:
(7*7)+(6*2)+(5*7)+(4*9)+(3*6)+(2*3)+(1*6)=162
162 % 10 = 2
So 72796-36-2 is a valid CAS Registry Number.

72796-36-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,4-trimethoxy-2-methylcyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,5-Cyclohexadien-1-one,3,4,4-trimethoxy-2-methyl

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:72796-36-2 SDS

72796-36-2Relevant academic research and scientific papers

CYCLOADDITIONS OF NON-STABILIZED AZOMETHINE YLIDES AND QUINONES SYNTHESIS OF THE RENIERA ISOINDOLE

Parker, Kathlyn A.,Cohen, Isaac D.,Padwa, Albert,Dent, William

, p. 4917 - 4920 (2007/10/02)

Azomethyne ylides, generated from cyanomethylamino silanes and excess silver fluoride, undergo cycloaddition with quinones to give, after oxidation in situ, quinonoid isoindoles.This reaction provides the key step for a short, high yield synthesis of the

Regiospecific Nucleophilic Aromatic Substitution: Conjugate Addition of Active Methylene Compounds to Quinone Monoacetals and Aromatization of the Adducts

Parker, Kathlyn A.,Kang, Suck-Ku

, p. 1218 - 1224 (2007/10/02)

Diethyl malonate adds to a variety of quinone monoacetals in a Michael reaction; acid-catalyzed loss of methanol and enolization converts the adducts to hydroquinone monoethers substituted ortho to the alkoxy substituent.The same sequence applied to ethyl

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