Detail of "6720-26-9"
- CAS Number:
- 6720-26-9
- Name:
[1,1'-Biphenyl]-2-carboxylicacid, 2'-formyl-
- Molecular Structure:
![Molecular Structure of 6720-26-9 ([1,1'-Biphenyl]-2-carboxylicacid, 2'-formyl-)](http://www.lookchem.com/300w/2010/069/6720-26-9.jpg)
- Formula:
- C14H10O3
- Molecular Weight:
- 226.23
- Synonyms:
- Diphenaldehydicacid (6CI,7CI,8CI);2-Formylbiphenyl-2'-carboxylic acid;2'-Formyl-[1,1'-biphenyl]-2-carboxylic acid;2'-Formylbiphenyl-2-carboxylicacid;
- Density:
- 1.264 g/cm3
- Melting Point:
- 128 °C
- Boiling Point:
- 413.2 °C at 760 mmHg
- Flash Point:
- 217.9 °C
- Hazard Symbols:
Xi
[1,1'-Biphenyl]-2-carboxylicacid, 2'-formyl-
Xi
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Reference
- Synthesis of some 2'-formylbiphenyl-2-carboxylic acid derivatives
- Synthesis of some 2'-formylbiphenyl-2-carboxylic acid derivatives.Several substances are used for example 6720-26-9 which is its cas registry number. Khalfina, I.Several substances are used for example 6720-26-9 which is its cas registry number. L.; Shabalina, G. N. (USSR). Izv. Tomsk. Politekh. Inst., 300, 102-4 (Russian) 1977. CODEN: ITPKAM. DOCUMENT TYPE: Journal CA Section: 25 (Noncondensed Aromatic Compounds) Section cross-reference(s): 5 Dry 2-HCOC6H4C6H4CO2H-2 reacted with ROH (R = Pr, Bu, Me2CHCH2) in the presence of H2SO4 to give ￡94% 2-HCOC6H4C6H4CO2R-2, which reacted with aq.-alc. HONH2 to give 74-96% 2-HON:CHC6H4C6H4CO2R-2 (I). All 3 I had fungicidal properties, with low toxicity in warm-blodded animals. ..
- Synthesis of some 2'-formylbiphenyl-2-carboxylic acid derivatives
- Synthesis of some 2'-formylbiphenyl-2-carboxylic acid derivatives.Several substances are used for example 6720-26-9 which is its cas registry number. Khalfina, I.Several substances are used for example 6720-26-9 which is its cas registry number. L.; Shabalina, G. N. (USSR). Izv. Tomsk. Politekh. Inst., 300, 102-4 (Russian) 1977. CODEN: ITPKAM. DOCUMENT TYPE: Journal CA Section: 25 (Noncondensed Aromatic Compounds) Section cross-reference(s): 5 Dry 2-HCOC6H4C6H4CO2H-2 reacted with ROH (R = Pr, Bu, Me2CHCH2) in the presence of H2SO4 to give ￡94% 2-HCOC6H4C6H4CO2R-2, which reacted with aq.-alc. HONH2 to give 74-96% 2-HON:CHC6H4C6H4CO2R-2 (I). All 3 I had fungicidal properties, with low toxicity in warm-blodded animals. ..