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ethyl 4-amino-3,5-dibromobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 58922-06-8 Structure
  • Basic information

    1. Product Name: ethyl 4-amino-3,5-dibromobenzoate
    2. Synonyms: ethyl 4-amino-3,5-dibromobenzoate;ethyl4-amino-3,5-dibromobenzoate(WXC08059);4-Amino-3,5-dibromobenzoic acid ethyl ester;Benzoic acid, 4-amino-3,5-dibromo-, ethyl ester
    3. CAS NO:58922-06-8
    4. Molecular Formula: C9H9Br2NO2
    5. Molecular Weight: 322.9813
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58922-06-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 373.4°C at 760 mmHg
    3. Flash Point: 179.6°C
    4. Appearance: N/A
    5. Density: 1.809g/cm3
    6. Vapor Pressure: 9E-06mmHg at 25°C
    7. Refractive Index: 1.614
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: ethyl 4-amino-3,5-dibromobenzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: ethyl 4-amino-3,5-dibromobenzoate(58922-06-8)
    12. EPA Substance Registry System: ethyl 4-amino-3,5-dibromobenzoate(58922-06-8)
  • 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: 58922-06-8(Hazardous Substances Data)

58922-06-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58922-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,2 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58922-06:
(7*5)+(6*8)+(5*9)+(4*2)+(3*2)+(2*0)+(1*6)=148
148 % 10 = 8
So 58922-06-8 is a valid CAS Registry Number.

58922-06-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-amino-3,5-dibromobenzoate

1.2 Other means of identification

Product number -
Other names 4-amino-3,5-dibromo-benzoic acid ethyl ester

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:58922-06-8 SDS

58922-06-8Relevant articles and documents

An Amine Functionalized Metal-Organic Framework as an Effective Catalyst for Conversion of CO2 and Biginelli Reactions

Verma, Ashish,De, Dinesh,Tomar, Kapil,Bharadwaj, Parimal K.

supporting information, p. 9765 - 9771 (2017/08/26)

A highly porous and thermally stable anionic Zn(II)-framework, {[(CH3)2NH2+]2[Zn3((μ3-O))(L)2(H2O)]·4DMF·2H2O}n (1), having exposed metal sites and pendant amine groups has been synthesized adopting the solvothermal technique. This anionic 3D framework showed two-fold interpenetration with 45.1% void volume. It has a 3,6-c binodal net with rare sit 3,6-conn topology. The metal bound aqua ligand could be easily removed along with the guest molecules in the lattice upon activation to afford the desolvated framework 1′. This produced exposed metal sites that, along with the pendant amine groups incorporated in the ligand, generated a coordination space in the framework to make it an outstanding heterogeneous catalyst for the chemical fixation of CO2 with various epoxides under atmospheric pressure and in the three-component Biginelli reaction with different aldehydes, ethyl acetoacetate, and urea to afford dihydropyrimidinones.

An easy and multigram-scale synthesis of versatile AA- and AB-type w-terphenylenes as building blocks for kinked polyphenylenes

Kissel, Patrick,Breitier, Simon,Reinmueller, Viktoria,Lanz, Patrick,Federer, Lukas,Schlueter, A. Dieter,Sakamoto, Junji

supporting information; experimental part, p. 2953 - 2955 (2009/11/30)

A set of m-terphenylenes having a readily functionalizable hydroxy group as well as either symmetric AA-type or unsymmetric AB-type halide termini have been prepared on a several-gram scale. The synthesis was carried out on the basis of the Suzuki-Miyaura

Stable Thioaminyl Radicals Having Functional Groups: Generation, ESR Spectra, Isolation, X-ray Crystallographic Analyses, and Magnetic Characterization of N-(Arylthio)-4-(ethoxycarbonyl)-2,6-diarylphenylaminyls, N-(Arylthio)-4-acetyl-2,6-diarylphenylaminyls, and N-(Arylthio)-4-cyano-2,6-diarylphenylaminyls

Miura, Yozo,Momoki, Masayoshi,Nakatsuji, Masaaki,Teki, Yoshio

, p. 1555 - 1565 (2007/10/03)

Oxidation of N-(arylthio)-4-(ethoxycarbonyl)-2,6-diarylanilines (9), N-(arylthio)-4-acetyl-2,6-diarylanilines (10), and N-(arylthio)-4-cyano-2,6-diarylanilines (11) with PbO2 yielded quite persistent N-(arylthio)-4-(ethoxycarbonyl)-2,6-diarylphenylaminyls(4), N-(arylthio)-4-acetyl-2,6-diarylphenylaminyls (5), and N-(arylthio)-4-cyano-2,6-diarylphenylaminyls (6), respectively, and they were isolated as pure radical crystals. On the other hand, N-(arylthio)-4-nitro-2,6-diarylphenylaminyls (6), and N-(arylthio)-4-chloro-2,6-diarylphenylaminyls (7), were unstable and soon decomposed. The X-ray crystallographic analyses of N-[(2,4-dichlorophenyl)thio]-4-acetyl-2,6-diphenylphenylaminyl (5c) and N-[(2,4-dichlorophenyl)thio]-4-cyano-2,6-diphenylphenylaminyl (6c) showed that the Ph-N-S-Ph π-framework is planar, and the 2- and 6-phenyl groups are twisted from the coplane. The ESR studies for 4-8 showed that their hyperfine coupling constants are nearly identical to each other and that the unpaired electron is extensively delocalized onto the anilino benzene ring and the arylthiyl group. The magnetic susceptibility measurements were carried out for five thioaminyl radical crystals and showed that one radical couples ferromagnetically with 2J/kB = 16.0 K, and the other four radicals couple antiferromagnetically with 2J/kB = -15.6 to -194.6 K or θ = -0.6 to -5.0 K.

Synthesis and Spectral Characterization of Blue Dyes of the Benzene Series

Thiel, W.,Mayer, R.,Jauer, E.-A.,Modrow, H.,Dost, H.

, p. 497 - 514 (2007/10/02)

53 Donor-acceptor substituted azo dyes of the benzene series were prepared by diazonium-coupling reactions (1a-s) or halogen-cyanide exchange (->2a-x, 3a-j).Described are the preparation of the amines 4a-m and the coupling compounds 5a-t and the procedure of diazotizing and coupling.The colouristic and spectroscopic data show that compounds of the general formula 1 are excellent brilliant blue azo dyes usefull for dyeing polyester material.

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