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97545-51-2

5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 5-[(2,5-dimethoxyanilino)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione

    Cas No: 97545-51-2

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  • 97545-51-2 Structure

  • Basic information

    1. Product Name: 5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE
    2. Synonyms: 5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE
    3. CAS NO:97545-51-2
    4. Molecular Formula: C15H17NO6
    5. Molecular Weight: 307.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97545-51-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(97545-51-2)
    11. EPA Substance Registry System: 5-(((2,5-DIMETHOXYPHENYL)AMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(97545-51-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 97545-51-2(Hazardous Substances Data)

97545-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97545-51-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,4 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 97545-51:
(7*9)+(6*7)+(5*5)+(4*4)+(3*5)+(2*5)+(1*1)=172
172 % 10 = 2
So 97545-51-2 is a valid CAS Registry Number.

97545-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-{[(2,5-dimethoxyphenylamino)]methylidene}-2,2-dimethyl-4,6-dioxo-1,3-dioxane

1.2 Other means of identification

Product number -
Other names 5-[(2,5-DIMETHOXYANILINO)METHYLENE]-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE

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:97545-51-2 SDS

97545-51-2Relevant articles and documents

An efficient synthesis of ([18F]fluoropropyl)quinoline-5,8- diones by rapid radiofluorination-oxidative demethylation

Sachin, Kalme,Jeong, Hwan-Jeong,Lim, Seok Tae,Sohn, Myung-Hee,Chi, Dae Yoon,Kim, Dong Wook

, p. 1763 - 1767 (2011)

Since many molecules bearing quinoline-5,8-dione or fused 1,4-quinone moieties possess a wide spectrum of biological activities, efficient methods for incorporation of fluorine-18 (F-18) into quinoline-5,8-diones have received considerable attention in po

Synthesis and biological activities of truncated acridone: Structure-activity relationship studies of cytotoxic 5-hydroxy-4-quinolone

Chun, Moon Woo,Olmstead, Kay Kim,Choi, Yong Suck,Lee, Chong Ock,Lee, Chong-Kyo,Kim, Joong Hyup,Lee, Jeewoo

, p. 789 - 792 (1997)

A series of 5-hydroxy-4-quinolone (3) and 5-methoxy-4-quinolone (4) derivatives were synthesized as truncated acridone analogues and evaluated for antitumor and antiherpes activities. Among them 5-hydroxy-8-methoxy-quinolone showed potent antitumor activi

Discovery of Mitochondrial Transcription Inhibitors Active in Pancreatic Cancer Cells

Chen, Wenmin,Hu, Shuai,Mao, Shuai,Xu, Yibin,Guo, Hui,Li, Haoxi,Paulsen, Michelle T.,Chen, Xinde,Ljungman, Mats,Neamati, Nouri

, p. 2029 - 2039 (2020/09/11)

Mitochondrial dysfunction is a hallmark of cancer cells and targeting cancer mitochondria has emerged as a promising anti-cancer therapy. Previously, we repurposed chlorambucil by conjugating it to a mitochondrial targeting triphenylphosphonium (TPP) grou

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 93, (2009/06/27)

Compounds of formula (I): wherein R4, R6 and R7 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 102-103, (2009/06/27)

Compounds of formula (I): wherein c, X, Y, R2, R4 and R5 are defined herein, are useful as inhibitors of HIV replication.

INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 100-101, (2009/06/27)

The present invention relates to compounds of formula (I) wherein c, X, Y, R2, R3, R4 and R6 are as defined herein, compositions and uses thereof for treating human immunodeficiency virus (HIV) infection. In particular, the present invention provides novel inhibitors of HIV integrase, pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HIV infection

Computational design, synthesis and biological evaluation of para-quinone-based inhibitors for redox regulation of the dual-specificity phosphatase Cdc25B

Keinan, Shahar,Paquette, William D.,Skoko, John J.,Beratan, David N.,Yang, Weitao,Shinde, Sunita,Johnston, Paul A.,Lazo, John S.,Wipf, Peter

experimental part, p. 3256 - 3263 (2009/02/05)

Quinoid inhibitors of Cdc25B were designed based on the Linear Combination of Atomic Potentials (LCAP) methodology. In contrast to a published hypothesis, the biological activities and hydrogen peroxide generation in reducing media of three synthetic models did not correlate with the quinone half-wave potential, E1/2.

Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof

-

Page/Page column 12, (2008/06/13)

Compositions for the oxidative dyeing of keratin fibers, comprising a medium suitable for dyeing and at least one bicyclic 6-6 (0:1, 0:2, 1:1, 1:2) aza heteroaromatic keratin dyeing compound with one or two N-oxides. A method for oxidative dyeing of kerat

SYNTHESIS OF 4(1H)-QUINOLONES BY THERMOLYSIS OF ARYLAMINOMETHYLENE MELDRUM'S ACID DERIVATIVES

Cassis, Raul,Tapia, Ricardo,Valderrama, Jaime A.

, p. 125 - 134 (2007/10/02)

A series of 4(1H)-quinolones were obtained from Meldrum's acid and arylamines in two steps.

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