METHYL 4-BENZYLOXYBENZOATE
Methyl 4-benzyloxybenzoate
CAS: 32122-11-5
Molecular Formula: C15H14O3
METHYL 4-BENZYLOXYBENZOATE - Names and Identifiers
| Name | Methyl 4-benzyloxybenzoate |
| Synonyms | RARECHEM AL BF 0087 LABOTEST-BB LT00455680 METHYL 4-BENZYLOXYBENZOATE Methyl 4-benzyloxybenzoate METHYL 4-BENZYLOXYBENZONATE 2-methyl-4-phenylmethoxybenzoate 4-BENZYLOXYBENZOIC ACID METHYL ESTER 4-Benzyloxybenzoic acid methyl ester METHYL 4-(BENZYLOXY)BENZENECARBOXYLATE 4-Methylbenzoicacidbenzyloxygenradicals |
| CAS | 32122-11-5 |
| InChI | InChI=1/C15H14O3/c1-17-15(16)13-7-9-14(10-8-13)18-11-12-5-3-2-4-6-12/h2-10H,11H2,1H3 |
METHYL 4-BENZYLOXYBENZOATE - Physico-chemical Properties
| Molecular Formula | C15H14O3 |
| Molar Mass | 242.27 |
| Density | 1.142g/cm3 |
| Melting Point | 99°C |
| Boling Point | 372.5°C at 760 mmHg |
| Flash Point | 156.2°C |
| Vapor Presure | 9.56E-06mmHg at 25°C |
| Maximum wavelength(λmax) | 257nm(MeOH)(lit.) |
| BRN | 2119212 |
| Storage Condition | Room Temprature |
| Refractive Index | 1.566 |
METHYL 4-BENZYLOXYBENZOATE - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| UN IDs | 3077 |
| HS Code | 29420000 |
METHYL 4-BENZYLOXYBENZOATE - Introduction
Methyl 4-benzyloxybenzoate, also known as Methyl 4-benzyloxy benzoate, chemical formula C15H14O3, is an organic compound.
Nature:
Methyl 4-benzyloxybenzoate is a colorless to yellowish liquid with a sweet, fruity flavor. It has a lower vapor pressure and a higher boiling point.
Use:
Methyl 4-benzyloxybenzoate is widely used in the chemical industry. It is an important fragrance and cosmetic ingredient commonly used in the formulation of perfumes, fragrances and cosmetics. In addition, it can also be used as an intermediate in organic synthesis for the synthesis of other organic compounds and drugs.
Method:
Methyl 4-benzyloxybenzoate can be obtained by reacting benzyl alcohol with Methyl p-hydroxybenzoate under alkaline conditions. The specific preparation method can refer to the relevant organic chemical synthesis manual.
Safety Information:
Methyl 4-benzyloxybenzoate is relatively safe under normal use and storage conditions. However, as an organic compound, it may cause irritation and allergic reactions to the human body. Therefore, it is necessary to pay attention to protective measures when using, avoid contact with skin, eyes and respiratory tract. In addition, it should be stored in a dry, well-ventilated place, away from fire and flammable substances. If necessary, refer to the relevant Safety Data Sheet for detailed safety information.
Nature:
Methyl 4-benzyloxybenzoate is a colorless to yellowish liquid with a sweet, fruity flavor. It has a lower vapor pressure and a higher boiling point.
Use:
Methyl 4-benzyloxybenzoate is widely used in the chemical industry. It is an important fragrance and cosmetic ingredient commonly used in the formulation of perfumes, fragrances and cosmetics. In addition, it can also be used as an intermediate in organic synthesis for the synthesis of other organic compounds and drugs.
Method:
Methyl 4-benzyloxybenzoate can be obtained by reacting benzyl alcohol with Methyl p-hydroxybenzoate under alkaline conditions. The specific preparation method can refer to the relevant organic chemical synthesis manual.
Safety Information:
Methyl 4-benzyloxybenzoate is relatively safe under normal use and storage conditions. However, as an organic compound, it may cause irritation and allergic reactions to the human body. Therefore, it is necessary to pay attention to protective measures when using, avoid contact with skin, eyes and respiratory tract. In addition, it should be stored in a dry, well-ventilated place, away from fire and flammable substances. If necessary, refer to the relevant Safety Data Sheet for detailed safety information.
Last Update：2024-04-09 20:45:29
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View History
METHYL 4-BENZYLOXYBENZOATE
1H-Pyrazole-3-carboxamide,5-nitro-(9CI)
4,5-Dichloroquinoline
R,S-Octane-1,2-diol
1H-Pyrazole-3-carboxamide,5-nitro-(9CI)
4,5-Dichloroquinoline
R,S-Octane-1,2-diol