N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE
4-(trifluoromethoxy)acetanilide
CAS: 1737-06-0
Molecular Formula: C9H8F3NO2
N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE - Names and Identifiers
| Name | 4-(trifluoromethoxy)acetanilide |
| Synonyms | 4-(TRIFLUOROMETHOXY)ACETANILIDE 4-(trifluoromethoxy)acetanilide 4'-(TRIFLUOROMETHOXY)ACETANILIDE N-[4-(trifluoromethoxy)phenyl]acetamide N-(4-(trifluoroMethoxy)phenyl)acetaMide N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE Acetamide, N-[4-(trifluoromethoxy)phenyl]- alpha,alpha,alpha-Trifluoro-p-acetanisidide p-Acetanisidide, alpha,alpha,alpha-trifluoro- |
| CAS | 1737-06-0 |
| InChI | InChI=1/C9H8F3NO2/c1-6(14)13-7-2-4-8(5-3-7)15-9(10,11)12/h2-5H,1H3,(H,13,14) |
N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE - Physico-chemical Properties
| Molecular Formula | C9H8F3NO2 |
| Molar Mass | 219.16 |
| Density | 1.345±0.06 g/cm3(Predicted) |
| Melting Point | 115-117°C |
| Boling Point | 296.8±40.0 °C(Predicted) |
| Flash Point | 133.3°C |
| Vapor Presure | 0.00141mmHg at 25°C |
| pKa | 14.14±0.70(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.496 |
N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| Hazard Class | IRRITANT |
N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE - Introduction
4-(trifluoromethoxy)acetanilide is an organic compound with the chemical formula C9H9F3NO2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 4-(trifluoromethoxy)acetanilide is a white crystal or crystalline powder.
-Solubility: It is soluble in organic solvents such as ethanol, chloroform and dichloromethane. Its solubility in water is relatively low.
-Stability: The compound is stable and not easy to decompose under regular storage conditions.
Use:
- 4-(trifluoromethoxy)acetanilide is mainly used for protecting group reactions in organic synthesis. It can be used as an introduction agent for a protecting group (commonly referred to as a "protecting Group"), which is used to protect certain functional groups in the compound during the reaction to avoid accidental chemical reactions.
-In addition, it can also be used to synthesize other organic compounds, such as drugs, dyes and pesticides.
Method:
The preparation method of -4-(trifluoromethoxy)acetanilide can be obtained by reacting 4-aminoacetanilide with methyl trifluoroformate. The reaction conditions generally require the use of base catalysis.
Safety Information:
-Since 4-(trifluoromethoxy)acetanilide is an organic compound, it should be treated with caution and avoid contact with skin and eyes.
-Good laboratory safety practices such as wearing protective gloves, goggles, and laboratory coats should be followed when using the compound.
-When using or handling this compound, maintain a well-ventilated working environment and avoid inhaling its gas or dust.
-According to the characteristics of chemicals, they should be stored properly, avoid contact with flammable substances, and keep away from open flames and high temperatures.
-During handling, care should be taken to avoid leakage and spillage of chemicals.
Nature:
-Appearance: 4-(trifluoromethoxy)acetanilide is a white crystal or crystalline powder.
-Solubility: It is soluble in organic solvents such as ethanol, chloroform and dichloromethane. Its solubility in water is relatively low.
-Stability: The compound is stable and not easy to decompose under regular storage conditions.
Use:
- 4-(trifluoromethoxy)acetanilide is mainly used for protecting group reactions in organic synthesis. It can be used as an introduction agent for a protecting group (commonly referred to as a "protecting Group"), which is used to protect certain functional groups in the compound during the reaction to avoid accidental chemical reactions.
-In addition, it can also be used to synthesize other organic compounds, such as drugs, dyes and pesticides.
Method:
The preparation method of -4-(trifluoromethoxy)acetanilide can be obtained by reacting 4-aminoacetanilide with methyl trifluoroformate. The reaction conditions generally require the use of base catalysis.
Safety Information:
-Since 4-(trifluoromethoxy)acetanilide is an organic compound, it should be treated with caution and avoid contact with skin and eyes.
-Good laboratory safety practices such as wearing protective gloves, goggles, and laboratory coats should be followed when using the compound.
-When using or handling this compound, maintain a well-ventilated working environment and avoid inhaling its gas or dust.
-According to the characteristics of chemicals, they should be stored properly, avoid contact with flammable substances, and keep away from open flames and high temperatures.
-During handling, care should be taken to avoid leakage and spillage of chemicals.
Last Update：2024-04-09 21:04:16
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View History
N1-[4-(TRIFLUOROMETHOXY)PHENYL]ACETAMIDE
tris(1-aziridinyl)phosphinesulphide
4-CHLOROINDOLE-2-CARBOHYDRAZIDE
2-氨基-8-乙基-4-甲基-6-(1H-吡唑-3-基)吡啶并[2,3-D]嘧啶-7(8H)-酮
Nortriptyline Hydrochloride Impurity J as Hydrochloride
N-叔丁氧羰基-3-哌啶酮
CARBONIC ACID BIS(2-METHOXYPHENYL) ESTER
RS-4-氟苯甘氨酸甲酯盐酸盐
4-chlorocinnamic acid
METHYL (S)-2-AMINO-3,3-DIMETHYLBUTYRATE HYDROCHLORIDE
tris(1-aziridinyl)phosphinesulphide
4-CHLOROINDOLE-2-CARBOHYDRAZIDE
2-氨基-8-乙基-4-甲基-6-(1H-吡唑-3-基)吡啶并[2,3-D]嘧啶-7(8H)-酮
Nortriptyline Hydrochloride Impurity J as Hydrochloride
N-叔丁氧羰基-3-哌啶酮
CARBONIC ACID BIS(2-METHOXYPHENYL) ESTER
RS-4-氟苯甘氨酸甲酯盐酸盐
4-chlorocinnamic acid
METHYL (S)-2-AMINO-3,3-DIMETHYLBUTYRATE HYDROCHLORIDE