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methyl 3,4-dibromobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 51329-16-9 Structure
  • Basic information

    1. Product Name: methyl 3,4-dibromobenzoate
    2. Synonyms: methyl 3,4-dibromobenzoate;3,4-Dibromobenzoic acid methyl ester
    3. CAS NO:51329-16-9
    4. Molecular Formula: C8H6Br2O2
    5. Molecular Weight: 293.94004
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 51329-16-9.mol
  • Chemical Properties

    1. Melting Point: 61-64 °C(Solv: ethyl ether (60-29-7); hexane (110-54-3))
    2. Boiling Point: 318.5±22.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.840±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 3,4-dibromobenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3,4-dibromobenzoate(51329-16-9)
    11. EPA Substance Registry System: methyl 3,4-dibromobenzoate(51329-16-9)
  • 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: 51329-16-9(Hazardous Substances Data)

51329-16-9 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 32, p. 1814, 1989 DOI: 10.1021/jm00128a025

Check Digit Verification of cas no

The CAS Registry Mumber 51329-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,2 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51329-16:
(7*5)+(6*1)+(5*3)+(4*2)+(3*9)+(2*1)+(1*6)=99
99 % 10 = 9
So 51329-16-9 is a valid CAS Registry Number.

51329-16-9Relevant articles and documents

Discovery of potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70

Vu, Chi B.,Corpuz, Evelyn G.,Merry, Taylor J.,Pradeepan, Selvaluxmi G.,Bartlett, Catherine,Bohacek, Regine S.,Botfield, Martyn C.,Eyermann, Charles J.,Lynch, Berkley A.,MacNeil, Ian A.,Ram, Mary K.,Van Schravendijk, Marie Rose,Violette, Shelia,Sawyer, Tomi K.

, p. 4088 - 4098 (2007/10/03)

A series of 1,2,4-oxadiazole analogues has been shown to be potent and selective SH2 inhibitors of the tyrosine kinase ZAP-70, a potential therapeutic target for immune suppression. These compounds typically are 200- 400-fold more potent than the native,

Biphenylcarboxamide derivatives as antagonists of platelet-activating factor

Tilley,Clader,Zawoiski,Wirkus,LeMahieu,O'Donnell,Crowley,Welton

, p. 1814 - 1820 (2007/10/02)

A series of N-[4-(3-pyridinyl)butyl]-1,1'-biphenyl-4-carboxamides was prepared, and the compounds were evaluated for platelet-activating factor (PAF) antagonist activity in a binding assay employing washed, whole dog platelets and in vivo for their abilit

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