4-AMINO-N-ISOPROPYLBENZAMIDE
- Product Name
- 4-AMINO-N-ISOPROPYLBENZAMIDE
- CAS No.
- 774-67-4
- Chemical Name
- 4-AMINO-N-ISOPROPYLBENZAMIDE
- Synonyms
- Isopropyl 4-aMinobenzaMide;4-AMINO-N-ISOPROPYLBENZAMIDE;Benzamide, 4-amino-N-(1-methylethyl)-;4-?Amino-?N-?(1-?methylethyl)?-benzamide;6-bromo-1,1-dioxo-1,2-benzothiazol-3-one;4-amino-N-isopropylbenzamide(SALTDATA: FREE)
- CBNumber
- CB41499135
- Molecular Formula
- C10H14N2O
- Formula Weight
- 178.23
- MOL File
- 774-67-4.mol
4-AMINO-N-ISOPROPYLBENZAMIDE Property
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- form
- solid
- Appearance
- Off-white to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H319Causes serious eye irritation
- Precautionary statements
-
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- CBR01240
- Product name
- 4-Amino-N-isopropylbenzamide
- Purity
- Aldrich
- Packaging
- 1g
- Price
- $107
- Updated
- 2025/07/31
- Product number
- I824185
- Product name
- Isopropyl4-aminobenzamide
- Packaging
- 500mg
- Price
- $65
- Updated
- 2021/12/16
- Product number
- 025833
- Product name
- 4-Amino-N-isopropylbenzamide
- Packaging
- 500mg
- Price
- $19
- Updated
- 2021/12/16
- Product number
- 025833
- Product name
- 4-Amino-N-isopropylbenzamide
- Packaging
- 1g
- Price
- $29
- Updated
- 2021/12/16
- Product number
- FA113857
- Product name
- 4-Amino-N-isopropylbenzamide
- Packaging
- 250mg
- Price
- $85
- Updated
- 2021/12/16
4-AMINO-N-ISOPROPYLBENZAMIDE Chemical Properties,Usage,Production
Synthesis
150-13-0
75-31-0
774-67-4
Synthesis of 4-amino-N-isopropylbenzamide (178.1). To a solution of p-aminobenzoic acid (177.1, 0.6 g, 4.37 mmol, 1.0 eq.) in DMF (6 mL) was sequentially added isopropylamine (0.73 mL, 8.75 mmol, 2.0 eq.) and HATU (2.49 g, 6.55 mmol, 1.5 eq.). After cooling the reaction mixture to 0 °C, DIPEA (1.4 mL, 8.74 mmol, 2.0 eq.) was slowly added at 0 °C. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the mixture was poured into water and the product was extracted with EtOAc (3 x 20 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography to afford 4-amino-N-isopropylbenzamide (178.1, 0.30 g, 38.5%) as a white solid.MS(ES): m/z 176.2 [M+H]+.
References
[1] Patent: WO2015/131080, 2015, A1. Location in patent: Paragraph 00957; 00958
[2] Journal of Medicinal Chemistry, 2007, vol. 50, # 20, p. 4898 - 4908
4-AMINO-N-ISOPROPYLBENZAMIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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