Benzoyl chloride is the common name. Its IUPAC name is benzene carbonyl chloride. aliquip ex ea commodo consequat.sed do eiusmod tempor incididunt ut quis labore et doliore magna aliqua.
Benzoyl chloride reacts with ammonia to form benzamide and ammonium chloride.
Benzyl chloride has a -CH2Cl group attached to the benzene ring, while benzoyl chloride has a -COCl group attached.
Benzoyl chloride reacts with water to form benzoic acid and hydrochloric acid.
nother name for benzoyl chloride is benzene carbonyl chloride.
99477 |
Synonym: 6-hydroxycoumarin, 6-hydroxy-2h-chromen-2-one, 2h-1-benzopyran-2-one, 6-hydroxy, 6-hydroxycoumaran, 2h-1-benzopyran-2-one,6-hydroxy, 6-hydroxbenzopyran-2-one, 6-hydroxy-2h-chromen-2-on, 6-hydroxycoumarine, 6-hydroxy coumarin, 6-hydroxy-2h-1-benzopyran-2-one
Quantity | 25g |
Melting Point | 249.0°C to 253.0°C |
Infrared Spectrum | Authentic |
Assay Percent Range | 97.5% min. (HPLC) |
Solubility Information | Solubility in water: insoluble. |
Formula Weight | 162.15 |
Percent Purity | 98% |
Chemical Name or Material | 6-Hydroxycoumarin |
6-Hydroxycoumarin, or umbelliferone, is a natural organic compound found in various plants, including chamomile, angelica, and parsley. This lactone derivative of coumarin is widely recognized for its remarkable biological and pharmacological activities.
One of the most notable features of 6-hydroxycoumarin is its fluorescent properties. The compound emits strong fluorescence when exposed to ultraviolet light, which has made it a valuable tool for researchers studying various biological molecules, such as enzymes, nucleic acids, and proteins.
Besides its fluorescence properties, 6-hydroxycoumarin has demonstrated anticoagulant, antioxidant, and anti-inflammatory properties. Traditional medicinal practices have employed this compound to alleviate various health issues, such as skin disorders, inflammation, and pain.
Researchers are now exploring the potential of 6-hydroxycoumarin as a lead compound for developing new drugs. It exhibits the ability to inhibit the growth of cancer cells and possesses neuroprotective properties, which could make it a promising candidate for treating cancer and neurological disorders.
6-hydroxycoumarin is a fascinating compound with diverse biological and pharmacological activities. Its fluorescent properties make it an essential tool for scientific research. At the same time, its potential as a lead compound for drug discovery opens up exciting avenues for developing new therapeutics.
 CASMin % |  97.5 |
 CAS Max % |  100.0 |
 Melting Point |  170°C to 172°C |
 Color |  Yellow to Brown |
 Infrared Spectrum |  Authentic |
 Assay Percent Range |  97.5% min. (HPLC) |
 Linear Formula |  H₂N[C₆H₃(F)COOH] |
 IUPAC Name |  2-amino-6-fluorobenzoic acid |
 Formula Weight |  155.13 |
 Percent Purity |  98% |
 Physical Form |  Crystalline Powder |
 Chemical Name or Material |  2-Amino-6-fluorobenzoic acid |
 Quantity |  1G/5G |
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Pictograms
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Hazard Classifications
Acute Tox. 4 Inhalation – Eye Irrit. 2 – Flam. Liq. 3 – STOT SE 3
Flash Point (C)
Closed cup
Signal Word
Warning
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Target Organs
Respiratory system
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Personal Protective Equipment
Dust mask type N95 (US), Eyeshields, Gloves
Precautionary Statements
P210 – P233 – P240 – P241 – P304 + P340 + P312 – P305 + P351 + P338
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Flash Point (F)
Closed cup