632340-58-0 Usage
Uses
Used in Organic Synthesis:
2-Amino-6-(bromomethyl)benzoic acid is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows for the development of new molecules with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Amino-6-(bromomethyl)benzoic acid is utilized as a key component in the design and synthesis of new drugs. Its presence in molecular structures can contribute to the pharmacological properties of these potential medications.
Used in Chemical Research:
2-Amino-6-(bromomethyl)benzoic acid is employed as a subject of study in chemical research to explore its reactivity, stability, and potential interactions with other compounds, which can lead to advancements in chemical science.
Used in Hazardous Chemical Management:
Given its classification as a hazardous chemical, 2-Amino-6-(bromomethyl)benzoic acid is also used in the development and implementation of safety protocols and handling procedures within laboratories and industrial settings to ensure the protection of personnel and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 632340-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,2,3,4 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 632340-58:
(8*6)+(7*3)+(6*2)+(5*3)+(4*4)+(3*0)+(2*5)+(1*8)=130
130 % 10 = 0
So 632340-58-0 is a valid CAS Registry Number.
632340-58-0Relevant academic research and scientific papers
An alternative method for the synthesis of γ-lactones by using cesium fluoride-celite/acetonitrile combination
Khan, Khalid Mohammed,Hayat, Safdar,Zia-Ullah,Atta-ur-Rahman,Iqbal-Choudhary,Maharvi, Ghulam Murtaza,Bayert, Ernst
, p. 3435 - 3453 (2007/10/03)
A variety of 2-(1-bromoalkyl) benzoic acids 4 undergo intramolecular nucleophilic substitution reaction when treated with a CsF-Celite as solid base in acetonitrile under reflux condition to give the corresponding cyclized phthalides in moderate to very good yield. These 2-(1-bromoalkyl) benzoic acids 4 are formed by the α-bromination of 2-alkylbenzoic acids 3 using N-bromosuccinimide and a catalytic amount of α,α′ -azoisobutyronitrile in carbon tetrachloride under reflux.
