ChemicalBook > CAS DataBase List > 4-AMINO-N-ISOPROPYLBENZAMIDE

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
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4-AMINO-N-ISOPROPYLBENZAMIDE Property

storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
Appearance
Off-white to yellow Solid
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Safety

Hazard Codes 
Xn
Risk Statements 
22-36-43
Safety Statements 
26
WGK Germany 
3
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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.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
CBR01240
Product name
4-Amino-N-isopropylbenzamide
Purity
Aldrich
Packaging
1g
Price
$107
Updated
2025/07/31
TRC
Product number
I824185
Product name
Isopropyl4-aminobenzamide
Packaging
500mg
Price
$65
Updated
2021/12/16
Matrix Scientific
Product number
025833
Product name
4-Amino-N-isopropylbenzamide
Packaging
500mg
Price
$19
Updated
2021/12/16
Matrix Scientific
Product number
025833
Product name
4-Amino-N-isopropylbenzamide
Packaging
1g
Price
$29
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA113857
Product name
4-Amino-N-isopropylbenzamide
Packaging
250mg
Price
$85
Updated
2021/12/16
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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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4-AMINO-N-ISOPROPYLBENZAMIDE Suppliers

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