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Benzyl anthranilate

Base Information
  • Chemical Name:Benzyl anthranilate
  • CAS No.:82185-41-9
  • Molecular Formula:C14H13NO2
  • Molecular Weight:227.263
  • Hs Code.:
  • European Community (EC) Number:279-911-2
  • DSSTox Substance ID:DTXSID10231606
  • Nikkaji Number:J284.152E
  • Wikidata:Q83112547
  • Mol file:82185-41-9.mol
Benzyl anthranilate

Synonyms:Benzyl anthranilate;Benzyl 2-aminobenzoate;82185-41-9;Benzoic acid, 2-amino-, phenylmethyl ester;2-Aminobenzoic acid benzyl ester;EINECS 279-911-2;Benzyl 2-aminobenzoate #;anthranilic acid benzyl ester;Oprea1_030897;SCHEMBL445585;DTXSID10231606;MFCD00060605;AKOS009144120;FS-4727;PHOSPHOENOLPYRUVICACIDMONOSODIUMSALT;B5249;CS-0456003;FT-0641850;A840267

Suppliers and Price of Benzyl anthranilate
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
  • Benzyl2-Aminobenzoate
  • 1g
  • $ 75.00
  • TCI Chemical
  • Benzyl Anthranilate >98.0%(GC)(T)
  • 1g
  • $ 34.00
  • TCI Chemical
  • Benzyl Anthranilate >98.0%(GC)(T)
  • 5g
  • $ 102.00
  • SynQuest Laboratories
  • Benzyl anthranilate 98%
  • 5 g
  • $ 81.00
  • SynQuest Laboratories
  • Benzyl anthranilate 98%
  • 1 g
  • $ 41.00
  • SynQuest Laboratories
  • Benzyl anthranilate 98%
  • 25 g
  • $ 321.00
  • Matrix Scientific
  • Benzyl anthranilate 98%
  • 10g
  • $ 138.00
  • Matrix Scientific
  • Benzyl anthranilate 98%
  • 25g
  • $ 320.00
  • Matrix Scientific
  • Benzyl anthranilate 98%
  • 50g
  • $ 470.00
  • Crysdot
  • Benzyl2-aminobenzoate 98%
  • 100g
  • $ 697.00
Total 54 raw suppliers
Chemical Property of Benzyl anthranilate
Chemical Property:
  • Vapor Pressure:7.57E-06mmHg at 25°C 
  • Melting Point:76 °C 
  • Refractive Index:1.618 
  • Boiling Point:375.8 °C at 760 mmHg 
  • Flash Point:215.1 °C 
  • PSA:52.32000 
  • Density:1.194 g/cm3 
  • LogP:3.20700 
  • Solubility.:soluble in Methanol 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:227.094628657
  • Heavy Atom Count:17
  • Complexity:249
Purity/Quality:

97% *data from raw suppliers

Benzyl2-Aminobenzoate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2N
  • Use Description Benzyl anthranilate is a versatile compound with applications in various fields. In the fragrance and flavor industry, it serves as a valuable ingredient, imparting a sweet, floral, and fruity scent. It is commonly used in perfumes, soaps, and cosmetics, enhancing their aromatic profiles. Additionally, benzyl anthranilate plays a role in the field of agriculture as a bird repellent. When applied to crops, it deters birds from feeding on the plants, protecting valuable agricultural yields. Its use as an avian repellent helps minimize crop damage caused by birds. In these ways, benzyl anthranilate contributes to the sensory experiences of consumers in the fragrance industry and aids in safeguarding agricultural produce from avian pests.
Technology Process of Benzyl anthranilate

There total 16 articles about Benzyl anthranilate 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 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.tet.2010.01.074
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.tet.2010.01.074
Guidance literature:
dmap; In N,N-dimethyl-formamide; at 60 ℃; for 2h;
DOI:10.1055/s-1982-29772
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