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1521-41-1,MFCD00017128
Catalog No.:AA006U9J

1521-41-1 | 3,4-Dimethoxybenzamide

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Purity
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Price(USD)
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250mg
98%
in stock  
$38.00   $27.00
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1g
98%
in stock  
$84.00   $59.00
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5g
98%
in stock  
$314.00   $220.00
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10g
98%
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$466.00   $327.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA006U9J
Chemical Name:
3,4-Dimethoxybenzamide
CAS Number:
1521-41-1
Molecular Formula:
C9H11NO3
Molecular Weight:
181.1885
MDL Number:
MFCD00017128
SMILES:
COc1cc(ccc1OC)C(=O)N
NSC Number:
370837
Properties
Properties
 
BP:
278.4°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
184  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
XLogP3:
1  

Downstream Synthesis Route

[1]ActaChimicaAcademiaeScientiarumHungaricae,1955,vol.6,p.323,330

[1]ChemicalCommunications,2013,vol.49,p.6060-6062

[2]Catalysisscienceandtechnology,2015,vol.5,p.1606-1622

[3]OrganicLetters,2014,vol.16,p.4866-4869

[4]OrganicSyntheses,1936,vol.16,p.4    Coll.Vol.,1943,vol.II,p.44

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1952,vol.72,p.1537    Chem.Abstr.,1953,p.10538

[1]JustusLiebigsAnnalenderChemie,1888,vol.244,p.72

[2]SyntheticCommunications,2012,vol.42,p.541-547

Literature

Title: Hansch analysis of veratric acid derivatives as antimicrobial agents.

Journal: European journal of medicinal chemistry 20090201

Title: Antibacterial alkoxybenzamide inhibitors of the essential bacterial cell division protein FtsZ.

Journal: Bioorganic & medicinal chemistry letters 20090115

Title: Synthesis and evaluation of cyclic secondary amine substituted phenyl and benzyl nitrofuranyl amides as novel antituberculosis agents.

Journal: Journal of medicinal chemistry 20051229

Title: Feng N, et, al. Amides produced by Streptoverticillium morookaense. SAGE Journals. 2007 Jan; 2(2):151-153.

Title: Pan Z, et, al. Preparation method of itopride hydrochloride. CN108610266A.

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SDS
Tags:1521-41-1 Molecular Formula|1521-41-1 MDL|1521-41-1 SMILES|1521-41-1 3,4-Dimethoxybenzamide