220362-31-2
3,4-difluoro-Benzeneethanamine
CAS: 220362-31-2
Molecular Formula: C8H9F2N
220362-31-2 - Names and Identifiers
220362-31-2 - Physico-chemical Properties
| Molecular Formula | C8H9F2N |
| Molar Mass | 157.16 |
| Density | 1.169 |
| Boling Point | 203℃ |
| Flash Point | 91℃ |
| Solubility | Acetonitrile (Slightly), Chloroform (Slightly) |
| Appearance | Oil |
| Color | Colourless |
| Storage Condition | 2-8°C(protect from light) |
220362-31-2 - Introduction
3, (3,) is an organic compound with the chemical formula C8H8F2N. Here are some properties, uses, methods, and safety information about 3:
Nature:
-Appearance: 3, is a colorless to light yellow liquid.
-Density: Its density is about 1.17g/cm³.
-Boiling point: 3, the boiling point is about 172-175 ° C.
-Solubility: It is soluble in many organic solvents, such as ethanol, ether and chloroform.
Use:
- 3, commonly used in the preparation of drugs and pesticides, as a synthetic intermediate.
-It can also be used for substitution reactions and selective addition reactions in organic synthesis reactions.
Method: The preparation of
3, 1-H is usually obtained by reacting 3,4-difluorophenylacetyl chloride (3,4-difluoro-benzyl chlide) with ammonia (N3) or ammonia water (h4oh).
Safety Information:
- 3, it is necessary to use appropriate safe operation methods. Personal protective equipment such as suitable gloves, safety glasses and protective clothing should be used.
-Avoid contact with the skin and inhalation of its vapors, as it may cause irritation and damage to the skin, eyes and respiratory system.
-When using and storing 3, the standard laboratory procedures should be followed to ensure safety.
Nature:
-Appearance: 3, is a colorless to light yellow liquid.
-Density: Its density is about 1.17g/cm³.
-Boiling point: 3, the boiling point is about 172-175 ° C.
-Solubility: It is soluble in many organic solvents, such as ethanol, ether and chloroform.
Use:
- 3, commonly used in the preparation of drugs and pesticides, as a synthetic intermediate.
-It can also be used for substitution reactions and selective addition reactions in organic synthesis reactions.
Method: The preparation of
3, 1-H is usually obtained by reacting 3,4-difluorophenylacetyl chloride (3,4-difluoro-benzyl chlide) with ammonia (N3) or ammonia water (h4oh).
Safety Information:
- 3, it is necessary to use appropriate safe operation methods. Personal protective equipment such as suitable gloves, safety glasses and protective clothing should be used.
-Avoid contact with the skin and inhalation of its vapors, as it may cause irritation and damage to the skin, eyes and respiratory system.
-When using and storing 3, the standard laboratory procedures should be followed to ensure safety.
Last Update：2024-04-09 02:00:44
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