2-Chlorobenzaldehyde
- CAS No. ：89-98-5
- Molecular Formula：C<sub>7</sub>H<sub>5</sub>ClO
- Purity：
- Molecular Weight：140.569
Product Details
pd_meltingpoint:9-11 °C(lit.)
Appearance:colourless to brown liquid
Perfect Factory Offer Excellent quality O-Chlorobenzaldehyde(OCBA) 89-98-5 with Safe Shipping
1.What is the 2-Chlorobenzaldehyde ?
2-Chlorobenzaldehyde is a colorless to yellowish liquid with a penetrating odor. Insoluble in water, soluble in benzene, alcohol and ether. 2-Chlorobenzaldehyde is considerably more resistant to oxidation than benzaldehyde. When it is heated with sodium sulfite solution under pressure, benzaldehyde-2-sulfonic acid forms.
2.What is the CAS number for 2-Chlorobenzaldehyde ?
The CAS number of 2-Chlorobenzaldehyde is 89-98-5.
3.What are another words for 2-Chlorobenzaldehyde ?
Synonyms for 2-Chlorobenzaldehyde 89-98-5:O-chlorobenzaldehyde (OCBA);2-Chloro benzaldehyde;Benzaldehyde,o-chloro- (8CI);
4.What is 2-Chlorobenzaldehyde (89-98-5) used for?
2-Chlorobenzaldehyde can be used to make alcohols, acids, and dyes; used in the rubber, tanning, and paper industries; used as an intermediate for optical brighteners, agricultural chemicals, and pharmaceuticals.It can also be used to prepare triphenyl methane and related dyes, organic intermediate.
InChI:InChI=1/C7H5ClO/c8-7-4-2-1-3-6(7)5-9/h1-5H
Relevant articles related to 2-Chlorobenzaldehyde:
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Transition metal-free oxidation of activated alcohols to aldehydes and ketones in 1,1,1,3,3,3-hexafluoro-2-propanol |
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Rerouting the Organocatalytic Benzoin Reaction toward Aldehyde Deuteration |
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2-chlorobenzaldehyde, a colorless to pale yellow solid with a strong almond aroma. It is an important organic synthesis intermediate widely used in the pharmaceutical, fragrance, and dye industries. Ortho chlorobenzaldehyde can be prepared by the oxidation reaction of ortho chlorotoluene, or by reacting ortho chlorobenzene with chlorine gas and sodium hydroxide. In organic synthesis, OCBA can serve as an aldehyde donor and participate in various chemical reactions, such as nucleophilic addition reactions, reduction reactions, and condensation reactions.
