Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3

6-Hydroxycoumarin | 6093-68-1

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Benzoyl chloride FAQS

What is the IUPAC name of benzoyl chloride?

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.

What happens when benzoyl chloride is treated with ammonia?

Benzoyl chloride reacts with ammonia to form benzamide and ammonium chloride.

What is the basic difference between benzyl chloride and benzoyl chloride?

Benzyl chloride has a -CH2Cl group attached to the benzene ring, while benzoyl chloride has a -COCl group attached.

What happens when benzoyl chloride reacts with water?

Benzoyl chloride reacts with water to form benzoic acid and hydrochloric acid.

What is another name for benzoyl chloride?

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.

specification

 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

technical service

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

SAFETY INFORMATION

Pictograms

GHS02, GHS07

 

Hazard Classifications


Acute Tox. 4 Inhalation – Eye Irrit. 2 – Flam. Liq. 3 – STOT SE 3

Flash Point (C)


Closed cup

Signal Word
Warning

 

Target Organs
Respiratory system

 

Personal Protective Equipment


Dust mask type N95 (US), Eyeshields, Gloves

Hazard Statements
H226, H319, H332, H335

 

WGK
WGK 1

Precautionary Statements


P210 – P233 – P240 – P241 – P304 + P340 + P312 – P305 + P351 + P338

 

Flash Point (F)
Closed cup