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1,1'-Ferrocenedicarboxylic acid / 1g

Purity: 97+%
Synonym: BIS(CARBOXYCYCLOPENTADIENYL)IRON; 1,1'-Dicarboxyferrocene Bis(carboxycyclopentadienyl)iron
Molecular Formula: C12H10FeO4
Molecular Weight: 274.06
SKU: MND-109006
CAS Number: 1293-87-4
MDL number: MFCD00001423
EC Number: 215-068-9
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 1g  
59.99 EUR



Safety Information


Hazard Statements

H302
H315
H319
H335

Precautionary Statements

P280
P270
P261
P271
P312
P264b
P302 + P352
P304 + P340
P305 + P351 + P338
P330
P362 + P364
P403 + P233
P501c

Pictograms



Properties

Melting Point>300°

 Product Description

1,1'-Ferrocenedicarboxylic acid is an organometallic compound containing a ferrocene core with two carboxylic acid functional groups. It is a solid material with applications in coordination chemistry and as a precursor for the synthesis of metal-organic frameworks.

 

Application:

1,1'-Ferrocenedicarboxylic acid is commonly used as a ligand in coordination chemistry reactions, forming stable complexes with transition metal ions. It is also utilized as a building block for the construction of metal-organic frameworks with potential applications in catalysis, gas storage, and drug delivery.

 

 

 

Articles:

- Nanoluminophores Composed of 1,1′-Ferrocenedicarboxylic Acid and Tetrakis-(4-carboxyphenyl) Porphyrin for Electrochemiluminescence Sensing

Publication Date: October 6, 2022

Peipei Li, Zhenjuan Xu, Lili Zhao, Haoyu Chen, Xiaohua Zhu, Youyu Zhang, Meiling Liu and Shouzhuo Yao

https://doi.org/10.1021/acsanm.2c03327

 

- N,C,N-chelated antimony(III), bismuth(III) and tin(IV) derivatives of 1,1′-ferrocenedicarboxylic acid

Publication Date: Available online 29 December 2016

R. Jambor, Z. Růžičková, M. Erben, L. Dostál

https://doi.org/10.1016/j.inoche.2016.12.008

 

- Synthesis and Cytotoxicity of the Dihydroartemisinin Ester of 1,1′-Ferrocenedicarboxylic Acid

Publication Date: 27 September 2021

S. U. Shaikhina, A. V. Semeikin, I. A. Gudovshchikov, T. I. Pavlik & N. L. Shimanovsky

https://doi.org/10.1007/s11094-021-02455-4