93-97-0
Chemical Structure
Benzoic anhydride
- CAS No.: 93-97-0
- Formula:C14H10O3
- Molecular Weight:226.23
IUPAC Name: benzoic anhydride
InChIKey: CHIHQLCVLOXUJW-UHFFFAOYSA-N
SMILES: O=C(OC(C1=CC=CC=C1)=O)C2=CC=CC=C2
Biological Activity: Benzoic anhydride is an aromatic acid anhydride organic small molecule that can serve as a catalyst or esterification reagent. Benzoic anhydride can hydrolyze to benzoic acid. Benzoic anhydride can catalyze the condensation polymerization of 2,5-dimethylpyrazine with 1,3,5-benzenetricarbaldehyde. Benzoic anhydride can be used in research related to organic synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Benzoic anhydride | 99.87% | Benzoic anhydride is an aromatic acid anhydride organic small molecule that can serve as a catalyst or esterification reagent. Benzoic anhydride can hydrolyze to benzoic acid. Benzoic anhydride can catalyze the condensation polymerization of 2,5-dimethylpyrazine with 1,3,5-benzenetricarbaldehyde. Benzoic anhydride can be used in research related to organic synthesis. | ||||||||||||||||||||
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Benzoic anhydride (Standard) | ≥98% | Benzoic anhydride (Standard) is the analytical standard of Benzoic anhydride (HY-Y1374). This product is intended for research and analytical applications. Benzoic anhydride is an aromatic acid anhydride organic small molecule that can serve as a catalyst or esterification reagent. Benzoic anhydride can hydrolyze to benzoic acid. Benzoic anhydride can catalyze the condensation polymerization of 2,5-dimethylpyrazine with 1,3,5-benzenetricarbaldehyde. Benzoic anhydride can be used in research related to organic synthesis. | ||||||||||||||||||||
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References
- [1]. Wang Z, et al. Green synthesis of olefin-linked covalent organic frameworks for hydrogen fuel cell applications. Nature communications. 2021 Mar 31;12(1):1982. [Content Brief]
- [2]. Liang W, et al. Lignin-based non-crosslinked nanocarriers: A promising delivery system of pesticide for development of sustainable agriculture. International journal of biological macromolecules. 2022 Nov 01;220:472-481.
- [3]. Erdmann L, et al. Synthesis and degradation characteristics of salicylic acid-derived poly(anhydride-esters). Biomaterials. 2000 Oct;21(19):1941-6.