89924-82-3
Chemical Structure
Cyclopropylcarboxylic acid-d4
Synonym(s): Carboxycyclopropane-d4; Cyclopropionic acid-d4
- CAS No.: 89924-82-3
- Formula:C4H2D4O2
- Molecular Weight:90.11
InChIKey: YMGUBTXCNDTFJI-LNLMKGTHSA-N
SMILES: O=C(C1C([2H])([2H])C1([2H])[2H])O
Biological Activity: Cyclopropylcarboxylic acid-d4 (Carboxycyclopropane-d4; Cyclopropionic acid-d4) is the deuterated-labeled Cyclopropylcarboxylic acid (HY-Y0001). Cyclopropylcarboxylic acid (Carboxycyclopropane; Cyclopropionic acid) is a small-molecule aliphatic carboxylic acid. Cyclopropylcarboxylic acid is also a common organic synthesis intermediate[1][3].
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Cyclopropylcarboxylic acid-d4 | 99.0% | Cyclopropylcarboxylic acid-d4 (Carboxycyclopropane-d4; Cyclopropionic acid-d4) is the deuterated-labeled Cyclopropylcarboxylic acid (HY-Y0001). Cyclopropylcarboxylic acid (Carboxycyclopropane; Cyclopropionic acid) is a small-molecule aliphatic carboxylic acid. Cyclopropylcarboxylic acid is also a common organic synthesis intermediate. | ||||||||||||||||||||
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Cyclopropylcarboxylic acid-d5 | Cyclopropylcarboxylic acid-d5 (Carboxycyclopropane-d5; Cyclopropionic acid-d5) is the deuterated-labeled Cyclopropylcarboxylic acid (HY-Y0001). Cyclopropylcarboxylic acid (Carboxycyclopropane; Cyclopropionic acid) is a small-molecule aliphatic carboxylic acid. Cyclopropylcarboxylic acid is also a common organic synthesis intermediate. | |||||||||||||||||||||
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Cyclopropylcarboxylic acid-d1 | Cyclopropylcarboxylic acid-d1 (Carboxycyclopropane-d1; Cyclopropionic acid-d1) is the deuterated-labeled Cyclopropylcarboxylic acid (HY-Y0001). Cyclopropylcarboxylic acid (Carboxycyclopropane; Cyclopropionic acid) is a small-molecule aliphatic carboxylic acid. Cyclopropylcarboxylic acid is also a common organic synthesis intermediate. | |||||||||||||||||||||
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Cyclopropylcarboxylic acid | 99.98% | Cyclopropylcarboxylic acid (Carboxycyclopropane; Cyclopropionic acid) is a small-molecule aliphatic carboxylic acid. Cyclopropylcarboxylic acid is also a common organic synthesis intermediate. | ||||||||||||||||||||
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References
- [1]. Katayama K, et al. Discovery and structure-activity relationships of spiroindolines as novel inducers of oligodendrocyte progenitor cell differentiation. Bioorganic & medicinal chemistry. 2020 Mar 15;28(6):115348.
- [3]. Boztaş M, et al. Synthesis and carbonic anhydrase isoenzymes I, II, IX, and XII inhibitory effects of dimethoxybromophenol derivatives incorporating cyclopropane moieties. J Med Chem. 2015 Jan 22;58(2):640-50.