1-Adamantanecarboxylic acid

1-Adamantanecarboxylic acid
Names
	Other names 1-Adamantane carboxylic acid
Identifiers
CAS Number	828-51-3 ;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL170568;
ChemSpider	12680;
ECHA InfoCard	100.011.440
EC Number	212-584-6;
PubChem CID	13235;
CompTox Dashboard (EPA)	DTXSID40870784 ;
	InChI InChI=1S/C11H16O2/c12-10(13)11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H,12,13) Key: JIMXXGFJRDUSRO-UHFFFAOYSA-N;
	SMILES C1C2CC3CC1CC(C2)(C3)C(=O)O;
Properties
Chemical formula	C11H16O2
Molar mass	180.247 g·mol−1
Appearance	white solid
Melting point	175–176.5 °C (347.0–349.7 °F; 448.1–449.6 K)
Related compounds
Related compounds	2-Adamantanecarboxylic acid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

1-Adamantanecarboxylic acid is an organic compound with the formula (CH₂)₆(CH)₃(CCO₂H). A white solid, it is the simplest carboxylic acid derivative of adamantane. The compound is notable for its synthesis by carboxylation of adamantane.^[1] 1-Adamantanecarboxylic acid is unusual in forming mononuclear tris(carboxylate) coordination complexes of the formula [M(O₂CR)₃]⁻ (M = Mn, Ni, Co, Zn).^[2]

References[edit]

^ H. Koch and W. Haaf (1964). "1-Adamantanecarboxylic Acid". Organic Syntheses. 44: 1. doi:10.15227/orgsyn.044.0001.
^ Fursova, E. Yu.; Romanenko, G. V.; Tolstikov, S. E.; Ovcharenko, V. I. (2019). "Mononuclear Transition Metal Adamantane-1-Carboxylates". Russian Chemical Bulletin. 68 (9): 1669–1674. doi:10.1007/s11172-019-2610-4. S2CID 203592748.

[1] H. Koch and W. Haaf (1964). "1-Adamantanecarboxylic Acid". Organic Syntheses. 44: 1. doi:10.15227/orgsyn.044.0001.

[2] Fursova, E. Yu.; Romanenko, G. V.; Tolstikov, S. E.; Ovcharenko, V. I. (2019). "Mononuclear Transition Metal Adamantane-1-Carboxylates". Russian Chemical Bulletin. 68 (9): 1669–1674. doi:10.1007/s11172-019-2610-4. S2CID 203592748.

[1]

[2]

See also[edit]

References[edit]