CAS 6307-82-0: Methyl 2-chloro-5-nitrobenzoate
Formula:C8H6ClNO4
InChI:InChI=1S/C8H6ClNO4/c1-14-8(11)6-4-5(10(12)13)2-3-7(6)9/h2-4H,1H3
InChI key:InChIKey=VCYWZLGOWNCJNJ-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC(N(=O)=O)=CC=C1Cl
Synonyms:- 2-Chloro-5-nitrobenzoic acid methyl ester
- Benzoic acid, 2-chloro-5-nitro-, methyl ester
- Brn 1966320
- Methylester kyseliny 2-chlor-5-nitrobenzoove
- Methylester kyseliny 2-chlor-5-nitrobenzoove [Czech]
- NSC 44287
- Methyl 2-chloro-5-nitrobenzoate
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Found 5 products.
Methyl 2-chloro-5-nitrobenzoate
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:215.58999633789062Methyl 2-chloro-5-nitrobenzoate
CAS:Methyl 2-chloro-5-nitrobenzoatePurity:99%Color and Shape:White PowderMolecular weight:215.59g/molMethyl 2-Chloro-5-nitrobenzoate
CAS:Formula:C8H6ClNO4Purity:>98.0%(GC)Color and Shape:White to Light yellow to Green powder to crystalMolecular weight:215.59Methyl 2-chloro-5-nitrobenzoate
CAS:Formula:C8H6ClNO4Purity:98%Color and Shape:SolidMolecular weight:215.5905Methyl 2-chloro-5-nitrobenzoate
CAS:Methyl 2-chloro-5-nitrobenzoate is a synthetic intermediate that can be used to synthesize benzimidazole derivatives. It is a deaminated compound and the yield of this reaction depends on the acidity of the reactants. In acidic conditions, methyl 2-chloro-5-nitrobenzoate yields more diazonium ions than in basic conditions. Methyl 2-chloro-5-nitrobenzoate reacts with benzyl chloride to form an iminium ion, which then reacts with potassium carbonate to produce the desired benzimidazole derivative. This reaction has been rationalized by proposing a mechanism in which the carbonyl group of methyl 2-chloro-5-nitrobenzoate is first protonated to form an enolate ion and then reacts with an electrophilic nucleophile (e.g., benzyl chloride) to produce the desired product.Purity:Min. 95%Ref: 3D-FM37867
Discontinued product
