12152-94-2
ferroceneboronic acid
CAS: 12152-94-2
Molecular Formula: C10H11BFeO210*
12152-94-2 - Names and Identifiers
| Name | ferroceneboronic acid |
| Synonyms | NSC 119337 FERROCENEBORONIC ACID ferroceneboronic acid Ferrocenylboronic acid ferrocenemetaboric acid (Boronocyclopentadienyl)cyclopentadienyl iron Ferroceneboronic acid (contains varying amounts of anhydride) N,N-dimethyl-3-(6,7,8,9-tetrahydropyrido[4,3-b]indol-5-yl)-1-propanamine dihydrochloride |
| CAS | 12152-94-2 |
| EINECS | 235-272-1 |
| InChI | InChI=1/C5H6BO2.C5H5.Fe/c7-6(8)5-3-1-2-4-5;1-2-4-5-3-1;/h1-4,7-8H;1-5H;/q2*-1;+2 |
12152-94-2 - Physico-chemical Properties
| Molecular Formula | C10H11BFeO210* |
| Molar Mass | 229.85 |
| Melting Point | 145-150 °C (dec.) (lit.) |
| Boling Point | 267.1°C at 760 mmHg |
| Flash Point | 115.3°C |
| Solubility | slightly sol. in Ether |
| Vapor Presure | 0.00113mmHg at 25°C |
| Appearance | powder to crystal |
| Color | White to Yellow to Orange |
| Storage Condition | 2-8℃ |
| MDL | MFCD00059074 |
12152-94-2 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves. |
| WGK Germany | 3 |
| HS Code | 29319090 |
12152-94-2 - Reference Information
| Use | Ferrocene boric acid, as a commercial reagent, can be used not only for the construction of carbon-carbon bonds, but also for boron-silicon bonds, Carbon-sulfur bonds and other chemical bonds containing heteroatoms. At the same time, compared with other ferrocene reagents, ferrocene boric acid has obvious advantages in reaction steps and atomic economy in transition metal-catalyzed coupling reactions. Therefore, ferrocene boric acid is widely used in the synthesis of ferrocene derivatives. |
| overview | the disclosure of ferrocene structure is an important breakthrough in the field of chemistry, which promoted the birth and development of modern metal organic chemistry. Ferrocene quickly attracted scientists to think about its fascinating chemical properties. Researchers began to develop synthetic methods using ferrocene derivatives and discovered their wide range of uses in the scientific field. In fact, more than 60 years after the discovery of ferrocene, ferrocene chemistry is still a very active research field. There are many reasons for this long-term sustained concern about ferrocene. First of all, ferrocene has a perfect sandwich structure, which breaks the traditional understanding of the nature of metal-carbon bonds. On the other hand, ferrocene and its derivatives show unusual stability to moisture, oxygen and many chemicals, as well as other unique electrochemical properties. At present, the commonly used reagents for introducing ferrocene groups into molecules include ferrocene, ferrocene formaldehyde, etc. The above reagents are mostly used for the formation of carbon-carbon bonds. |
Last Update：2024-04-10 22:29:15
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View History
12152-94-2
Diethanolamine Hydrochloride
N-(3-aminophenyl)propanamide
2483830-06-2
O-(4-Nitrobenzyl)hydroxylamine hydrochloride
2-Fluoro-4-formylbenzoic acid
64034-01-1
LYPRESSIN
AMYL BENZOATE
UNII-EFY6W0M8TG
Diethanolamine Hydrochloride
N-(3-aminophenyl)propanamide
2483830-06-2
O-(4-Nitrobenzyl)hydroxylamine hydrochloride
2-Fluoro-4-formylbenzoic acid
64034-01-1
LYPRESSIN
AMYL BENZOATE
UNII-EFY6W0M8TG