165018
Methyl 5-chlorosalicylate
97%
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Empirical Formula (Hill Notation):
C8H7ClO3
CAS Number:
Molecular Weight:
186.59
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
46-50 °C (lit.)
functional group
chloro
ester
SMILES string
COC(=O)c1cc(Cl)ccc1O
InChI
1S/C8H7ClO3/c1-12-8(11)6-4-5(9)2-3-7(6)10/h2-4,10H,1H3
InChI key
KJWHRMZKJXOWFC-UHFFFAOYSA-N
Related Categories
General description
Methyl 5-chlorosalicylate on iodination yields 3-iodo-5-chlorosalicylate.
Application
Methyl 5-chlorosalicylate was used in the synthesis of N-p-methoxyphenylbenzimino-p-chloro-o-carbomethoxyphenyl ether.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
411. Some derivatives of diphenylamine and a new synthesis of N-arylanthranilic acids and of acridones.
Jamison MM and Turner EE.
Journal of the Chemical Society, 1954-1959 (1937)
Halogenosalicylohydroxamic Acids. I. Dihalogenosalicylohydroxamic Acids.
DUDA H, et al.
Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques, 13(5), 341-347 (1965)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service