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Allyl 2-aminobenzoate

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Identification
Molecular formula
C10H11NO2
CAS number
7492-74-6
IUPAC name
allyl 2-aminobenzoate
State
State

At room temperature, allyl 2-aminobenzoate is in a liquid state, characterized by a slightly oily texture.

Melting point (Celsius)
-42.00
Melting point (Kelvin)
231.15
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.15
General information
Molecular weight
177.21g/mol
Molar mass
177.2050g/mol
Density
1.1245g/cm3
Appearence

Allyl 2-aminobenzoate is typically an oily liquid with a faint aromatic odor. It tends to have a pale yellow to colorless appearance.

Comment on solubility

Solubility of Allyl 2-Aminobenzoate

Allyl 2-aminobenzoate, with its unique structure, exhibits intriguing solubility characteristics. This compound is typically regarded as:

  • Moderately soluble in organic solvents: Due to the presence of both hydrophilic amino and hydrophobic allyl groups, it can effectively dissolve in a range of organic solvents.
  • Limited solubility in water: The presence of the amino group suggests some potential for hydrogen bonding with water; however, the overall hydrophobic nature reduces its solubility.

In summary, when assessing the solubility of allyl 2-aminobenzoate, it is paramount to consider:

  1. The solvent's nature: Nonpolar and mildly polar solvents tend to enhance solubility.
  2. Temperature: An increase in temperature may lead to an increase in solubility due to enhanced molecular movement.

In general, while allyl 2-aminobenzoate may not be highly soluble in aqueous solutions, its favorable interactions with organic solvents make it a versatile compound in various chemical applications.

Interesting facts

Interesting Facts About Allyl 2-Aminobenzoate

Allyl 2-aminobenzoate, a compound belonging to the class of esters, has several fascinating attributes that make it noteworthy for researchers and students alike. Here are some key highlights:

  • Structure and Reactivity: This compound features an allyl group attached to an amino benzoate structure. The presence of both the amino and the ester functional groups grants it unique reactivity, opening doors for various chemical transformations.
  • Natural Occurrence: It can be related to natural compounds, as many esters and amino acids exist in nature. These connections make it essential in studying biochemical pathways and natural product synthesis.
  • Applications: Allyl 2-aminobenzoate is often explored for its potential in pharmaceutical applications, including drug formulation and development. Its versatility may also find applications in the manufacturing of perfumes due to its pleasant scent profile.
  • Polymer Chemistry: The reactivity of the allyl group allows this compound to participate in polymerization processes. It can be a starting material for the synthesis of more complex polymers with varied properties.
  • Environmental Considerations: Numerous research studies are ongoing to assess the environmental impact of such compounds. Understanding their behavior can lead to the development of safer, more sustainable chemical processes.

In the words of a renowned chemist, "The beauty of chemistry lies in its ability to connect the dots between seemingly distant substances." With allyl 2-aminobenzoate, this statement resonates deeply, as its structural uniqueness and versatile applications continue to engage minds in the field.

As further studies unfold, it becomes increasingly clear that allyl 2-aminobenzoate is more than just a chemical entity; it is a gateway to exploring a myriad of chemical interactions and applications.

Synonyms
ALLYL ANTHRANILATE
7493-63-2
Allyl 2-aminobenzoate
2-Propenyl 2-aminobenzoate
Anthranilic acid, allyl ester
Allyl O-aminobenzoate
2-Propen-1-yl anthranilate
Vinyl carbinyl anthranilate
Benzoic acid, 2-amino-, 2-propenyl ester
FEMA No. 2020
2-Propen-1-yl 2-aminobenzoate
CCRIS 6207
EINECS 231-331-0
NSC 147476
DTXSID3024441
AI3-36005
prop-2-en-1-yl 2-aminobenzoate
UNII-81T0041N82
NSC-147476
DTXCID804441
81T0041N82
ALLYL ANTHRANILATE [FHFI]
ALLYL ANTHRANILATE [USP-RS]
Anthranilic acid, allyl ester (8CI)
BENZOIC ACID, 2-AMINO-, 2-PROPEN-1-YL ESTER
ALLYL ANTHRANILATE (USP-RS)
2-AMINOBENZOIC ACID, ALLYL ESTER
231-331-0
inchi=1/c10h11no2/c1-2-7-13-10(12)8-5-3-4-6-9(8)11/h2-6h,1,7,11h
ucanfcxakymfga-uhfffaoysa-n
prop-2-enyl 2-aminobenzoate
Allyl Anthraniliate
Allyl 2-aminobenzoate #
Allyl anthranilate, >=98%
MLS002415710
SCHEMBL759012
CHEMBL1606698
2-amino-benzoic acid allyl ester
CHEBI:178980
HMS3039M08
HAA49363
Tox21_201129
NSC147476
NCGC00091858-01
NCGC00091858-02
NCGC00258681-01
AS-87943
SMR001370893
CAS-7493-63-2
Benzoic acid,2-amino-,2-propen-1-yl ester
NS00022749
H37421
Q27269266
Allyl anthranilate, United States Pharmacopeia (USP) Reference Standard