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5-Bromonicotinamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 28733-43-9 Structure
  • Basic information

    1. Product Name: 5-Bromonicotinamide
    2. Synonyms: 5-bromo-3-pyridinecarboxamid;5-bromo-nicotinamid;BUTTPARK 146\04-27;IFLAB-BB F2124-0064;5-BROMO-3-PYRIDINECARBOXAMIDE;AKOS BBS-00003123;5-BROMONICOTINAMIDE;5-BROMOPYRIDINE-3-CARBOXAMIDE
    3. CAS NO:28733-43-9
    4. Molecular Formula: C6H5BrN2O
    5. Molecular Weight: 201.02
    6. EINECS: 244-065-5
    7. Product Categories: blocks;Bromides;Carboxes;Pyridines;Pyridine;Pyridine Series;Heterocyclic Compounds
    8. Mol File: 28733-43-9.mol
  • Chemical Properties

    1. Melting Point: 219-223 °C
    2. Boiling Point: 315.5 °C at 760 mmHg
    3. Flash Point: 144.6 °C
    4. Appearance: Off-white to light pink/Powder
    5. Density: 1.71 g/cm3
    6. Vapor Pressure: 0.000435mmHg at 25°C
    7. Refractive Index: 1.613
    8. Storage Temp.: Inert atmosphere,Room Temperature
    9. Solubility: N/A
    10. PKA: 14.21±0.50(Predicted)
    11. CAS DataBase Reference: 5-Bromonicotinamide(CAS DataBase Reference)
    12. NIST Chemistry Reference: 5-Bromonicotinamide(28733-43-9)
    13. EPA Substance Registry System: 5-Bromonicotinamide(28733-43-9)
  • Safety Data

    1. Hazard Codes: Xn,Xi
    2. Statements: 22-36/37/38
    3. Safety Statements: 26-36-37/39
    4. WGK Germany: 3
    5. RTECS: QS4170000
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 28733-43-9(Hazardous Substances Data)

28733-43-9 Usage

Chemical Properties

Off-white to light pink powder

Synthesis Reference(s)

Journal of Medicinal Chemistry, 20, p. 129, 1977 DOI: 10.1021/jm00211a027

Check Digit Verification of cas no

The CAS Registry Mumber 28733-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,3 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 28733-43:
(7*2)+(6*8)+(5*7)+(4*3)+(3*3)+(2*4)+(1*3)=129
129 % 10 = 9
So 28733-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrN2O/c7-5-1-4(6(8)10)2-9-3-5/h1-3H,(H2,8,10)

28733-43-9 Well-known Company Product Price

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  • TCI America

  • (B3536)  5-Bromonicotinamide  >98.0%(GC)

  • 28733-43-9

  • 5g

  • 990.00CNY

  • Detail
  • Alfa Aesar

  • (A17840)  5-Bromonicotinamide, 98%   

  • 28733-43-9

  • 5g

  • 223.0CNY

  • Detail
  • Alfa Aesar

  • (A17840)  5-Bromonicotinamide, 98%   

  • 28733-43-9

  • 25g

  • 1085.0CNY

  • Detail
  • Alfa Aesar

  • (A17840)  5-Bromonicotinamide, 98%   

  • 28733-43-9

  • 100g

  • 2948.0CNY

  • Detail
  • Aldrich

  • (667137)  5-Bromo-3-pyridinecarboxamide  97%

  • 28733-43-9

  • 667137-5G

  • 341.64CNY

  • Detail
  • Aldrich

  • (667137)  5-Bromo-3-pyridinecarboxamide  97%

  • 28733-43-9

  • 667137-25G

  • 1,140.75CNY

  • Detail

28733-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromopyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 5-Bromo-3-pyridinecarboxamide

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:28733-43-9 SDS

28733-43-9Relevant articles and documents

Corresponding amine nitrile and method of manufacturing thereof

-

Paragraph 0135; 0136; 0137; 0146, (2018/05/07)

The invention relates to a manufacturing method of nitrile. Compared with the prior art, the manufacturing method has the characteristics of significantly reduced using amount of an ammonia source, low environmental pressure, low energy consumption, low production cost, high purity and yield of a nitrile product and the like, and nitrile with a more complex structure can be obtained. The invention also relates to a method for manufacturing corresponding amine from nitrile.

Supported Gold Nanoparticles-Catalyzed Microwave-Assisted Hydration of Nitriles to Amides under Base-Free Conditions

Kumar, Sandeep,Sharma, Saurabh,Das, Pralay

supporting information, p. 2889 - 2894 (2016/09/16)

Polystyrene-supported gold (Au@PS) nanoparticles were synthesized by the reduction deposition approach and well characterized by UV-visible, XRD, TEM, SAED, EDX, and XPS studies. The Au@PS was applied as catalyst for the hydration of nitriles to amides in water under microwave irradiation. Several functionalized aromatic, heterocyclic and aliphatic nitriles were found to be active for synthesis of the corresponding amides where no activation of water by base, ligand and support is needed. Easy recovery, negligible leaching and recyclability for up to eight runs are added advantages of the catalyst under water-mediated reaction conditions. (Figure presented.).

Discovery of 7-aryl-substituted (1,5-naphthyridin-4-yl)ureas as Aurora kinase inhibitors

Defaux, Julien,Antoine, Maud,Le Borgne, Marc,Schuster, Tilmann,Seipelt, Irene,Aicher, Babette,Teifel, Michael,Guenther, Eckhard,Gerlach, Matthias,Marchand, Pascal

, p. 217 - 232 (2014/01/17)

As part of our research projects to identify new chemical entities of biological interest, we developed a synthetic approach and the biological evaluation of (7-aryl-1,5-naphthyridin-4-yl)ureas as a novel class of Aurora kinase inhibitors for the treatment of malignant diseases based on pathological cell proliferation. 1,5-Naphthyridine derivatives showed excellent inhibitory activities toward Aurora kinases A and B, and the most active compound, 1-cyclopropyl-3-[7-(1-methyl-1H-pyrazol-4-yl)-1,5-naphthyridin-4-yl]urea (49), displayed IC50 values of 13 and 107 nM against Aurora kinases A and B, respectively. In addition, the selectivity toward a panel of seven cancer-related protein kinases was highlighted. In vitro ADME properties were also determined in order to rationalize the difficulties in correlating antiproliferative activity with Aurora kinase inhibition. Finally, the good safety profile of these compounds imparts promising potential for their further development as anticancer agents. Promising Aurora inhibitors: Herein we report a series of (7-aryl-1,5-naphthyridin-4-yl)ureas as a novel class of nanomolar-range Aurora kinase inhibitors. The described derivatives have good cell-penetration parameters and safety profiles, but their efficiency toward signaling pathways are insufficient to induce cell death. We also highlight their selectivity toward a panel of seven cancer-related protein kinases. Copyright

GLYCAN ANALYSIS USING DEUTERATED GLUCOSE

-

Page/Page column 54; 56, (2008/06/13)

Novel Methods and apparatuses are provided for use in identifying glucose metabolic products and determining metabolic flux by administering D7-glucose to a subject.

NOVEL AZALIDE AND AZALACTAM DERIVATIVES AND PROCESS FOR THE PRODUCTION OF THE SAME

-

Page/Page column 46, (2010/11/08)

A compound represented by the following general formula (1) or a pharmaceutically acceptable salt thereof, which is useful for a prophylactic and/or therapeutic treatment of a microbial infectious disease. [R1 is hydrogen atom, or a linear C1-6 alkylcarbonyl group; R2 is hydrogen atom, or a C1-6 alkylcarbonyl group; R3 is hydrogen atom, a C1-6 alkyl group, a C1-6 alkylcarbonyl group, a C1-6 alkenyl group, a C2-6 alkenylcarbonyl group, a C2-6 alkynyl group, or an Ar-B- group (Ar represents an aryl group, or a heterocyclic group, and B is a C1-6 alkyl group, a C1-6 alkylcarbonyl group, a C2-6 alkenyl group, a C2-6 alkenylcarbonyl group, or a C2-6 alkynyl group); R5, R6, R7, and R8 represent hydrogen atom, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, or an Ar-B'- group (B' is a C1-6 alkyl group, a C2-6 alkenyl group, or a C2-6 alkynyl group); X is oxygen atom, or an -NR4- group (R4 is hydrogen atom, a C1-6 alkyl group, or a C1-6 alkyl group which may be substituted with an Ar group); and R4' is hydrogen atom, or a group represented by the aforementioned formula (a) (R3" and R4" represent hydrogen atom, or a linear or branched C1-6 alkylcarbonyl group)]

SUBSTITUTED THIAZOLE DERIVATIVES BEARING 3-PYRIDYL GROUPS, PROCESS FOR PREPARING THE SAME AND USE THEREOF

-

Page/Page column 61, (2008/06/13)

The present invention provides a pharmaceutical composition having a steroid C17,20-lyase inhibitory activity, which is useful as a prophylactic or therapeutic agent of prostatism, tumor such as breast cancer and the like, more particularly, a steroid C17,20-lyase inhibitor containing a compound represented by the formula: wherein A1 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, one of A2 and A3 is a hydrogen atom, a halogen atom, a C1-4 aliphatic hydrocarbon group optionally having substituents or an optionally esterified carboxyl group, the other of A2 and A3 is an aromatic hydrocarbon group optionally having substituents or a heterocyclic group optionally having substituents, and at least one of A1, A2 and A3 is a 3-pyridyl group optionally having substituents, or a salt thereof or a prodrug thereof.

Selective cyclooxygenase-2 inhibitors: Heteroaryl modified 1,2-diarylimidazoles are potent, orally active antiinflammatory agents

Khanna,Yu,Huff,Weier,Xu,Koszyk,Collins,Cogburn,Isakson,Koboldt,Masferrer,Perkins,Seibert,Veenhuizen,Yuan,Yang,Zhang

, p. 3168 - 3185 (2007/10/03)

A series of heteroaryl modified 1,2-diarylimidazoles has been synthesized and found to be potent and highly selective (1000-9000-fold) inhibitors of the human COX-2.3-Pyridyl derived COX-2 selective inhibitor (25) exhibited excellent activity in acute (carrageenan induced paw edema, ED50 = 5.4 mg/kg) and chronic (adjuvant induced arthritis, ED50 = 0.25 mg/kg) models of inflammation. The relatively long half-life of 25 in rat and dog prompted investigation of the pyridyl and other heteroaromatic systems containing potential metabolic functionalities. A number of substituted pyridyl and thiazole containing compounds (e.g., 44, 46, 54, 76, and 78) demonstrated excellent oral activity in every efficacy model evaluated. Several orally active diarylimidazoles exhibited desirable pharmacokinetics profiles and showed no GI toxicity in the rat up to 100 mg/kg in both acute and chronic models. The paper describes facile and practical syntheses of the targeted diarylimidazoles. The structure-activity relationships and antiinflammatory properties of a series of diarylimidazoles are discussed.

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