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Benzoic acid, 6-amino-2,3-dimethoxy-, also known as 6-amino-2,3-dimethoxybenzoic acid, is an organic compound with the chemical formula C9H11NO4. It is a derivative of benzoic acid, featuring an amino group at the 6th position, and two methoxy groups attached to the 2nd and 3rd carbon atoms. Benzoic acid, 6-amino-2,3-dimethoxy- is a white crystalline solid and is soluble in water, ethanol, and other organic solvents. It has various applications in the pharmaceutical and chemical industries, such as a building block for the synthesis of pharmaceuticals, dyes, and other organic compounds. Due to its unique structure, it exhibits interesting chemical properties and reactivity, making it a valuable compound for research and development purposes.

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  • 5653-51-0 Structure
  • Basic information

    1. Product Name: Benzoic acid, 6-amino-2,3-dimethoxy-
    2. Synonyms:
    3. CAS NO:5653-51-0
    4. Molecular Formula: C9H11NO4
    5. Molecular Weight: 197.191
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5653-51-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzoic acid, 6-amino-2,3-dimethoxy-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 6-amino-2,3-dimethoxy-(5653-51-0)
    11. EPA Substance Registry System: Benzoic acid, 6-amino-2,3-dimethoxy-(5653-51-0)
  • 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: 5653-51-0(Hazardous Substances Data)

5653-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5653-51-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5653-51:
(6*5)+(5*6)+(4*5)+(3*3)+(2*5)+(1*1)=100
100 % 10 = 0
So 5653-51-0 is a valid CAS Registry Number.

5653-51-0Relevant articles and documents

ANTIBACTERIAL COMPOUNDS

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Page/Page column 192; 193, (2013/04/24)

The present Invention relates to cephalosporin antibacterial compounds of Formula (!): corresponding pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions, compound preparation and treatment methods for bacterial infections, especially those caused by gram-negative bacteria.

NEW DS DNA BINDING FLUORESCENT DYES

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Page/Page column 29; Sheet 8, (2008/12/05)

The present invention is directed to a fluorescent dye comprising a benzothiazolium moiety and a pyrimidinium moiety connected by a mono-methine bridge, characterized in that (i) the 2-position of the pyrimidine carries a substituent which starts with a C

FUSED-RING PYRIMIDIN-4(3H)-ONE DERIVATIVES, PROCESSES FOR THE PREPARATION AND USES THEREOF

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Page 298, (2010/02/06)

AbstractNovel compounds of the following formula (I) and pharmacologically acceptable salt and esters thereof can modulate LXR function and as a result show excellent anti-arteriosclerotic and anti-inflammatory activity:wherein:A represents aryl or heteroaryl;R1, R2 and R3 are the same or different and each represents hydrogen, hydroxyl, nitro, cyano, amino, halogen, carboxy, carbamoyl, mercapto, alkyl, haloalkyl, alkylcarbonyloxy, alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylamino, dialkylamino, alkylcarbonylamino, N-(alkylcarbonyl)-N-(alkyl)amino, alkoxycarbonylamino, N-(alkoxycarbonyl)-N-(alkyl)amino, alkylsulfonylamino, N-(alkylsulfonyl)-N-(alkyl)amino, haloalkylsulfonylamino, N-(haloalkylsulfonyl)-N-(alkyl)amino, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl or dialkylaminocarbonyl group, or R1 and R2 together are alkylenedioxy;R4 and R5 are the same or different and each represents hydrogen, hydroxyl, amino, halogen, mercapto, alkyl, haloalkyl, alkoxy, alkoxycarbonyl or alkylthio;X represents hydrogen, hydroxyl, halogen, alkoxy or haloalkoxy; andY represents an optionally substituted alkyl, cycloalkyl, heterocyclyl, aryl, cycloalkylalkyl, heterocyclylalkyl or aralkyl group.

Substituted quinazolinediones

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, (2008/06/13)

The synthesis of 5,6-dioxy substituted quinazolinediones is described. The novel quinazolinediones are useful as cardiotonic agents.

Substituted 5,6-dialkoxyquinazoline derivatives

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, (2008/06/13)

Quinazoline derivatives having an oxy substituent in 5 and 6 positions are described. The novel quinazoline derivatives are useful as cardiotonic agents.

Process for the preparation of 5,6-dialkoxyanthranilic acids

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, (2008/06/13)

A process for the preparation of 5,6-dialkoxyanthranilic acids is described. The 5,6-dialkoxyanthranilic acids are useful in the preparation of substituted quinazolinediones which are active cardiotonic agents.

A Regioselective Entry to 13-Substituted 8-Oxoprotoberberines. Total Synthesis of (+/-)-Corydaline

Saa, Carlos,Guitian, Enrique,Castedo, Luis,Suau, Rafael,Saa, Jose Manuel

, p. 2781 - 2784 (2007/10/02)

13-Alkyl and 13-aryl substituted 8-oxoprotoberberines were obtained by interamolecular benzyne cycloaddition of isoquinolinopyrrolinediones with arynes.This convergent and highly regioselective reaction has been applied to the synthesis of (+/-)-corydalin

Synthesis of 2-(Alkylamino)-5,6- and -6,7-dihydroxy-3,4-dihydroquinazolines and Evaluation as Potential Dopamine Agonists

Grosso, John A.,Nichols, David E.,Kohli, Jai D.,Glock, Dana

, p. 703 - 708 (2007/10/02)

Based upon the known dopaminergic properties of 2-aminodihydroxy-1,2,3,4-tetrahydronaphthalenes (ADTN's), heterocyclic congengers were prepared.Several 2-(alkylamino)-5,6- and -6,7-dihydroxy-3,4-dihydroquinazolines were synthesized and tested for a dopami

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