Methyl 4-amino-2-chlorobenzoate

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Products Intro: Product Name:4-Amino-2-chlorobenzoic acid methyl ester
CAS:46004-37-9
Purity:98%(Min,GC) Package:1G;1KG;100KG
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Products Intro: Product Name: Methyl 4-amino-2-chlorobenzoate
CAS:46004-37-9
Purity:99% Package:1kg;8USD
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Products Intro: Product Name:4-Amino-2-chlorobenzoic acid methyl ester
CAS:46004-37-9
Purity:97% Package:10G 100G 1KG 25KG
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Products Intro: Product Name:methyl 4-amino-2-chlorobenzoate
CAS:46004-37-9
Purity:98% Package:5KG;1KG
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Products Intro: CAS:46004-37-9

Methyl 4-amino-2-chlorobenzoate manufacturers
Methyl 4-amino-2-chlorobenzoate Basic information
Product Name:Methyl 4-amino-2-chlorobenzoate
Synonyms:methyl 4-amino-2-chlorobenzoate(SALTDATA: FREE);AKOS BB-3102;Methyl 4-amino-2-chlorobenzoate 2-Chioro-4-aminobenzoic acid methyl ester;METHYL 4-AMINO-2-CHLOROBENZOATE;2-chioro-4-aminobenzoic acid methyl ester;4-AMINO-2-CHLORO-BENZOIC ACID METHYL ESTER;2-chloro-4-amino benzoic acid methyl ester;Methyl 2-Chloro-4-Aminobenzoate
CAS:46004-37-9
MF:C8H8ClNO2
MW:185.61
EINECS:
Product Categories:Aromatic Esters;Phenylacetic acid;Miscellaneous;Benzenes
Mol File:46004-37-9.mol
Methyl 4-amino-2-chlorobenzoate Structure
Methyl 4-amino-2-chlorobenzoate Chemical Properties
Melting point 112-114°C
Boiling point 334.2±22.0 °C(Predicted)
density 1.311±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Chloroform
form powder to crystal
pka1.41±0.10(Predicted)
color White to Almost white
InChIInChI=1S/C8H8ClNO2/c1-12-8(11)6-3-2-5(10)4-7(6)9/h2-4H,10H2,1H3
InChIKeyDSHBGNPOIBSIOQ-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC=C(N)C=C1Cl
CAS DataBase Reference46004-37-9(CAS DataBase Reference)
Safety Information
HS Code 2916399090
MSDS Information
Methyl 4-amino-2-chlorobenzoate Usage And Synthesis
Chemical Propertiesoff white powder
UsesMethyl 4-Amino-2-chlorobenzoate is used as a reagent to synthesize selective LXR agonists that increase HDL levels and reverse cholesterol transport in mice.
References[1] Patent: WO2010/65760, 2010, A1. Location in patent: Page/Page column 150
[2] Journal of Medicinal Chemistry, 2010, vol. 53, # 4, p. 1546 - 1562
[3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 17, p. 4377 - 4381
[4] Acad. romine Stud. Cerc. Chim., 1956, vol. 4, p. 175,177
[5] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 13, p. 2991 - 3013
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