29823-18-5
29823-18-5
Chemical Structure
Ethyl 7-bromoheptanoate
- CAS No.: 29823-18-5
- Formula:C9H17BrO2
- Molecular Weight:237.13
IUPAC Name: ethyl 7-bromoheptanoate
InChIKey: OOBFNDGMAGSNKA-UHFFFAOYSA-N
SMILES: CCOC(=O)CCCCCCBr
Biological Activity: Ethyl 7-bromoheptanoate is a key intermediate and alkylating agent that can be used in the synthesis of other active compounds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Ethyl 7-bromoheptanoate | 99.55% | Ethyl 7-bromoheptanoate is a key intermediate and alkylating agent that can be used in the synthesis of other active compounds. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.96
HY-346388-Bromocaprylic acid ethyl ester -
Similarity Score 0.95
HY-W041970Ethyl 6-bromohexanoate -
Similarity Score 0.90
HY-W088478Methyl 8-bromooctanoate -
Similarity Score 0.90
HY-32088Ethyl 10-bromodecanoate -
Similarity Score 0.89
HY-W236653Ethyl 7-aminoheptanoate -
Similarity Score 0.89
HY-W004688Methyl 7-bromoheptanoate -
Similarity Score 0.89
HY-W015305Ethyl octanoate -
Similarity Score 0.87
HY-22035Ethyl 7-aminoheptanoate hydrochloride -
Similarity Score 0.87
HY-W088462Methyl 9-bromononanoate -
Explore the MedChemAI to find more analogs
References
- [1]. Canonica S, et al. A Convenient Preparation of Etiwl 7-Bromoheptanoate. Organic Preparations and Procedures International, 1989, 21(2): 253-254.
- [2]. Cai X, et al. Discovery of 7-(4-(3-ethynylphenylamino)-7-methoxyquinazolin-6-yloxy)-N-hydroxyheptanamide (CUDc-101) as a potent multi-acting HDAC, EGFR, and HER2 inhibitor for the treatment of cancer. J Med Chem. 2010 Mar 11;53(5):2000-9. [Content Brief]
