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2-[(4-METHOXYANILINO)METHYLENE]-1,3-CYCLOHEXANEDIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62370-45-0

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62370-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62370-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,7 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62370-45:
(7*6)+(6*2)+(5*3)+(4*7)+(3*0)+(2*4)+(1*5)=110
110 % 10 = 0
So 62370-45-0 is a valid CAS Registry Number.

62370-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methoxyanilino)methylidene]cyclohexane-1,3-dione

1.2 Other means of identification

Product number -
Other names 10N-525S

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:62370-45-0 SDS

62370-45-0Relevant academic research and scientific papers

New approaches for the synthesis of heterocyclic compounds derived from cyclohexan-1,3-dione with anti-proliferative activities

Masoud, Ayat Ali,Milad, Yara Raafat,Mohareb, Rafat Milad

, p. 72 - 87 (2021/06/07)

In the present work a series of heterocyclization reactions were adopted using cyclohexan-1,3-dione through its reaction with either furan-2-carbaldehyde or thiophene-2-carbaldehyde to give the corresponding ylidene derivatives 3a,b. The latter compounds underwent heterocyclization reactions to give thiophene and pyran derivatives 5a–d and 6a–d, respectively. Moreover, compounds 3a,b reacted with elemental sulfur and phenyl isothiocyanate to give the fused thiazole derivatives 8a,b. In addition, the reaction with either of hydrazine hydrate or phenylhydrazine has given the 4-hydrazo-no-4,5,6,7-tetrahydro-2H-indazole derivatives 10a–d, respectively. Similarly, the reaction of either 3a or 3b with hydroxylamine hydrochloride gave the 6,7-dihydrobenzo[c]isoxazol-4(5H)-one oxime derivatives 12a and 12b, respectively. Other fused heterocyclic compounds were produced and their structures were elucidated. Evaluation of the synthesized compounds against selected cancer cell lines was performed. The most active compounds were further evaluated against tyrosine kinases and Pim-1 kinase inhibitions.

Metal-free coupling/isomerization reaction of isocyanide and cyclic 1,3-dione: A selective Csp3-H functionalization strategy for C-C bond formation

Jiang, Hui,Li, Jian,Li, Yefei,Sun, Mingming,Yao, Jun

supporting information, (2020/08/28)

A metal-free oxidative coupling/isomerization reaction of isocyanide and cyclic 1, 3-dione has been disclosed. In the presence of di-tert-butylperoxide (DTBP), a series of isocyanides are subjected to reaction with subsituted 1, 3-diones for direct synthe

Silver-Catalyzed Cross-Coupling of Isocyanides and Active Methylene Compounds by a Radical Process

Liu, Jianquan,Liu, Zhenhua,Liao, Peiqiu,Zhang, Lin,Tu, Tao,Bi, Xihe

supporting information, p. 10618 - 10622 (2015/09/02)

Isocyanides are versatile building blocks, and have been extensively exploited in C-H functionalization reactions. However, transition-metal-catalyzed direct C-H functionalization reactions with isocyanides suffer from over-insertion of isocyanides. Repor

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