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69818-23-1

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69818-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69818-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,1 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69818-23:
(7*6)+(6*9)+(5*8)+(4*1)+(3*8)+(2*2)+(1*3)=171
171 % 10 = 1
So 69818-23-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6O3/c1-10-5-2-3-6(8)7(9)4-5/h2-4H,1H3

69818-23-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxycyclohexa-3,5-diene-1,2-dione

1.2 Other means of identification

Product number -
Other names 4-Methoxy-1,2-benzoquinone

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:69818-23-1 SDS

69818-23-1Relevant articles and documents

Biomimetic Hydroxylation Catalysis Through Self-Assembly of a Bis(pyrazolyl)methane Copper-Peroxo Complex

Wilfer, Claudia,Liebh?user, Patricia,Erdmann, Hannes,Hoffmann, Alexander,Herres-Pawlis, Sonja

, p. 494 - 502 (2015)

We synthesised and characterised four copper complexes (with copper in the oxidation states I and II) with the bis(pyrazolyl) methane ligands HC(3-tBuPz)2(Py) and HC(3-tBuPz)2-(Qu). With the quinolinyl ligand (2-quinolinyl)bis(3-tert

A Catalyst-Controlled Aerobic Coupling of ortho-Quinones and Phenols Applied to the Synthesis of Aryl Ethers

Huang, Zheng,Lumb, Jean-Philip

, p. 11543 - 11547 (2016/11/17)

ortho-Quinones are underutilized six-carbon-atom building blocks. We herein describe an approach for controlling their reactivity with copper that gives rise to a catalytic aerobic cross-coupling with phenols. The resulting aryl ethers are generated in high yield across a broad substrate scope under mild conditions. This method represents a unique example where the covalent modification of an ortho-quinone is catalyzed by a transition metal, creating new opportunities for their utilization in synthesis.

Bioinspired organocatalytic aerobic C-H oxidation of amines with an ortho -quinone catalyst

Qin, Yan,Zhang, Long,Lv, Jian,Luo, Sanzhong,Cheng, Jin-Pei

supporting information, p. 1469 - 1472 (2015/03/30)

A simple bioinspired ortho-quinone catalyst for the aerobic oxidative dehydrogenation of amines to imines is reported. Without any metal cocatalysts, the identified optimal ortho-quinone catalyst enables the oxidations of α-branched primary amines and cyclic secondary amines. Mechanistic studies have disclosed the origins of different performances of ortho-quinone vs para-quinone in biomimetic amine oxidations.

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