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5-BROMO-2-HYDRAZINOBENZOIC ACID

Base Information
  • Chemical Name:5-BROMO-2-HYDRAZINOBENZOIC ACID
  • CAS No.:177192-82-4
  • Molecular Formula:C7H7BrN2O2
  • Molecular Weight:231.049
  • Hs Code.:2928000090
  • Mol file:177192-82-4.mol
5-BROMO-2-HYDRAZINOBENZOIC ACID

Synonyms:5-BROMO-2-HYDRAZINOBENZOIC ACID;4-Bromo-2-carboxyphenylhydrazine

Suppliers and Price of 5-BROMO-2-HYDRAZINOBENZOIC ACID
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 5-Bromo-2-hydrazinobenzoicAcid
  • 100mg
  • $ 175.00
  • SynQuest Laboratories
  • 5-Bromo-2-hydrazinobenzoic acid
  • 500 mg
  • $ 224.00
  • Apolloscientific
  • 5-Bromo-2-hydrazinobenzoicacid
  • 500mg
  • $ 203.00
  • American Custom Chemicals Corporation
  • 5-BROMO-2-HYDRAZINOBENZOIC ACID 95.00%
  • 500MG
  • $ 781.24
  • American Custom Chemicals Corporation
  • 5-BROMO-2-HYDRAZINOBENZOIC ACID 95.00%
  • 1G
  • $ 941.33
  • Alichem
  • 5-Bromo-2-hydrazinylbenzoicacid
  • 1g
  • $ 1460.20
  • Alichem
  • 5-Bromo-2-hydrazinylbenzoicacid
  • 500mg
  • $ 839.45
  • Alichem
  • 5-Bromo-2-hydrazinylbenzoicacid
  • 250mg
  • $ 470.40
Total 2 raw suppliers
Chemical Property of 5-BROMO-2-HYDRAZINOBENZOIC ACID
Chemical Property:
  • PSA:75.35000 
  • LogP:2.20620 
Purity/Quality:

97% *data from raw suppliers

5-Bromo-2-hydrazinobenzoicAcid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 5-BROMO-2-HYDRAZINOBENZOIC ACID

There total 1 articles about 5-BROMO-2-HYDRAZINOBENZOIC ACID which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; tin(ll) chloride; sodium nitrite;
DOI:10.1016/j.bmcl.2015.04.101
Guidance literature:
Multi-step reaction with 6 steps
1: acetone / Reflux
2: 1,2-dichloro-ethane; benzotriazol-1-ol; ammonium hydroxide / tetrahydrofuran; dichloromethane
3: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / Reflux
4: sodium hydroxide; water / methanol; tetrahydrofuran
5: 1,2-dichloro-ethane; benzotriazol-1-ol
6: tetrakis(triphenylphosphine) palladium(0); sodium carbonate / toluene; methanol; water
With ammonium hydroxide; tetrakis(triphenylphosphine) palladium(0); water; sodium carbonate; benzotriazol-1-ol; 1,2-dichloro-ethane; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; acetone; toluene; 6: |Suzuki Coupling;
DOI:10.1016/j.bmcl.2015.04.101
Guidance literature:
Multi-step reaction with 8 steps
1: acetone / Reflux
2: 1,2-dichloro-ethane; benzotriazol-1-ol; ammonium hydroxide / tetrahydrofuran; dichloromethane
3: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / Reflux
4: sodium hydroxide; water / methanol; tetrahydrofuran
5: diphenyl phosphoryl azide; triethylamine
6: trifluoroacetic acid / dichloromethane
7: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / water; 1,2-dimethoxyethane
8: N-ethyl-N,N-diisopropylamine; 1,2-dichloro-ethane; benzotriazol-1-ol / N,N-dimethyl-formamide
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; ammonium hydroxide; diphenyl phosphoryl azide; water; sodium carbonate; benzotriazol-1-ol; 1,2-dichloro-ethane; triethylamine; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium hydroxide; In tetrahydrofuran; methanol; 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene; 5: |Curtius Rearrangement / 7: |Suzuki Coupling;
DOI:10.1016/j.bmcl.2015.04.101
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