ChemicalBook > CAS DataBase List > 3-CHLORO-4-ISOPROPOXY-BENZOIC ACID

3-CHLORO-4-ISOPROPOXY-BENZOIC ACID

Product Name
3-CHLORO-4-ISOPROPOXY-BENZOIC ACID
CAS No.
213598-07-3
Chemical Name
3-CHLORO-4-ISOPROPOXY-BENZOIC ACID
Synonyms
Ozanimod Impurity 51;3-CHLORO-4-ISOPROPOXY-BENZOIC ACID;3-chloro-4-propan-2-yloxybenzoic Acid;3-Chloro-4-(1-methylethoxy)benzoic acid;Benzoic acid, 3-chloro-4-(1-methylethoxy)-
CBNumber
CB7841404
Molecular Formula
C10H11ClO3
Formula Weight
214.65
MOL File
213598-07-3.mol
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3-CHLORO-4-ISOPROPOXY-BENZOIC ACID Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C598313
Product name
3-Chloro-4-isopropoxybenzoicAcid
Packaging
100mg
Price
$65
Updated
2021/12/16
ChemScene
Product number
CS-M0439
Product name
3-chloro-4-isopropoxybenzoicacid
Packaging
1g
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC150050
Product name
3-Chloro-4-isopropoxybenzoicacid
Packaging
250mg
Price
$75
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC150050
Product name
3-Chloro-4-isopropoxybenzoicacid
Packaging
500mg
Price
$100
Updated
2021/12/16
AK Scientific
Product number
0859AB
Product name
3-Chloro-4-isopropoxybenzoicacid
Packaging
1g
Price
$158
Updated
2021/12/16
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3-CHLORO-4-ISOPROPOXY-BENZOIC ACID Chemical Properties,Usage,Production

Synthesis

916596-04-8

213598-07-3

Step 2: Synthesis of 3-chloro-4-isopropoxybenzoic acid (34). To a stirred solution of 3-chloro-4-isopropoxybenzonitrile (33, 57 g, 291 mmol) in ethanol (EtOH, 120 mL) was added an aqueous 12% potassium hydroxide (KOH) solution (300 mL), and the reaction mixture was heated to 100 °C and kept for 3 h. The reaction was carried out with the addition of aqueous potassium hydroxide (KOH). Upon completion of the reaction, the mixture was cooled to room temperature and acidified with hydrochloric acid (HCl) to pH 5. A yellow solid precipitated during the acidification process, which was collected by filtration, washed with water and dried. The resulting solid was mixed with hexane, stirred for 5 minutes and decanted to remove the hexane. The process was repeated once, and the solid was resuspended in hexane, filtered, and washed with hexane to give 3-chloro-4-isopropoxybenzoic acid (34) as a white solid (45 g, 72% yield).

References

[1] Patent: WO2017/4609, 2017, A1. Location in patent: Paragraph 0277
[2] Patent: WO2017/4608, 2017, A1. Location in patent: Paragraph 0153

3-CHLORO-4-ISOPROPOXY-BENZOIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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3-CHLORO-4-ISOPROPOXY-BENZOIC ACID Suppliers

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213598-07-3, 3-CHLORO-4-ISOPROPOXY-BENZOIC ACIDRelated Search:


  • 3-chloro-4-propan-2-yloxybenzoic Acid
  • 3-CHLORO-4-ISOPROPOXY-BENZOIC ACID
  • Benzoic acid, 3-chloro-4-(1-methylethoxy)-
  • 3-Chloro-4-(1-methylethoxy)benzoic acid
  • Ozanimod Impurity 51
  • 213598-07-3