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369398-78-7

5-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)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-[(1,3-benzodioxol-5-ylamino)methylidene]-2,2-dimethyl-1,3-dioxane-4,6-dione

    Cas No: 369398-78-7

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  • 369398-78-7 Structure

  • Basic information

    1. Product Name: 5-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE
    2. Synonyms: 5-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE;5-{[(2H-1,3-benzodioxol-5-yl)amino]methylidene}-2,2-dimethyl-1,3-dioxane-4,6-dione
    3. CAS NO:369398-78-7
    4. Molecular Formula: C14H13NO6
    5. Molecular Weight: 291.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 369398-78-7.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-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(369398-78-7)
    11. EPA Substance Registry System: 5-((BENZO[3,4-D]1,3-DIOXOLEN-5-YLAMINO)METHYLENE)-2,2-DIMETHYL-1,3-DIOXANE-4,6-DIONE(369398-78-7)

  • 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: 369398-78-7(Hazardous Substances Data)

369398-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 369398-78-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,3,9 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 369398-78:
(8*3)+(7*6)+(6*9)+(5*3)+(4*9)+(3*8)+(2*7)+(1*8)=217
217 % 10 = 7
So 369398-78-7 is a valid CAS Registry Number.

369398-78-7SDS

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 5-((benzo[d][1,3]dioxol-5-ylamino)methylene)-2,2-dimethyl-1,3-dioxane-4,6-dione

1.2 Other means of identification

Product number -
Other names 5-[(1,3-BENZODIOXOL-5-YLAMINO)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:369398-78-7 SDS

369398-78-7Relevant articles and documents

Direct C-3-alkenylation of quinolones via palladium-catalyzed C-H functionalization

Li, Mingzong,Li, Liangxi,Ge, Haibo

supporting information; experimental part, p. 2445 - 2449 (2010/12/25)

An unprecedented C-3-alkenylation of quinolones was reported through palladium-catalyzed C-H functionalization with 1% catalyst loading. This method provides an efficient route to a variety of new quinolone derivatives.

Synthesis and biological evaluation of new heterocyclic quinolinones as anti-parasite and anti-HIV drug candidates

Darque, Albert,Dumetre, Aurelien,Hutter, Sebastien,Casano, Gilles,Robin, Maxime,Pannecouque, Christophe,Azas, Nadine

supporting information; experimental part, p. 5962 - 5964 (2010/06/17)

We have synthesized quinolinones with potential antiparasitic and anti-HIV activities by an original two-step method involving microwave irradiation and have evaluated their activities against Plasmodium falciparum, Leishmania donovani, Trichomonas vaginalis, and HIV. None of the tested compounds had been previously described using this method of synthesis. One of the compounds had interesting antiparasitic and anti-HIV activity, which could be improved by substitution with different radicals.

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