221622-80-6

Basic information

• Product Name: 5-Chloro-2-fluoro-4-methoxy-benzaldehyde
• Synonyms: Benzaldehyde, 5-chloro-2-fluoro-4-methoxy-
• CAS NO: 221622-80-6
• Molecular Formula: C₈H₆ClFO₂
• Molecular Weight: 188.5834432
• Mol File: 221622-80-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Chloro-2-fluoro-4-methoxy-benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Chloro-2-fluoro-4-methoxy-benzaldehyde(221622-80-6)
• EPA Substance Registry System: 5-Chloro-2-fluoro-4-methoxy-benzaldehyde(221622-80-6)

Safety Data

• Hazardous Substances Data: 221622-80-6(Hazardous Substances Data)

Upstream product

• 331-64-6 2-fluoro-4-methoxy-benzaldehyde 

Downstream Products

• 1340476-15-4 2-(5-chloro-2-fluoro-4-methoxyphenyl)acetic acid 
• 1340476-14-3 2-(5-chloro-2-fluoro-4-methoxyphenyl)-2-hydroxyacetonitrile 
• 793670-65-2 5-chloro-2-fluoro-4-methoxy-3-nitro-benzaldehyde 

Relevant articles and documents

BENZO[b]THIOPHENE COMPOUNDS AS STING AGONISTS

Compounds of general formula (Ia), compounds of general formula (Ia′), compounds of general formula (Ib), compounds of general formula (Ib′), compounds of general formula (I), compounds of general formula (I′), and their pharmaceutically acceptable salts,

Iodide-catalyzed reductions: Development of a synthesis of phenylacetic acids

A new convenient and scalable synthesis of phenylacetic acids has been developed via the iodide catalyzed reduction of mandelic acids. The procedure relies on in situ generation of hydroiodic acid from catalytic sodium iodide, employing phosphorus acid as the stoichiometric reductant.

BENZOXAZINONE DERIVATIVES HAVING AFFINITY FOR 5- HT RECEPTORS, THEIR PREPARATION AND USE

Benzoxazinone derivatives, their preparation and use Compounds of formula (I) and pharmaceutically acceptable salts thereof are disclosed: (I) wherein R1 is hydrogen or C1-6alkyl; R2 is fluoro or chloro; R3 is hydrogen, fluoro or chloro; and X is nitrogen