[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE
CAS: 109376-35-4
Molecular Formula: C22H22BrO2P
[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide - Names and Identifiers
[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide - Physico-chemical Properties
| Molecular Formula | C22H22BrO2P |
| Molar Mass | 431.3 |
| Melting Point | 152-154°C(lit.) |
| Storage Condition | 2-8°C |
[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide - 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. S37/39 - Wear suitable gloves and eye/face protection |
| WGK Germany | 3 |
[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide - Introduction
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is an organic compound with the chemical formula (C2H5OC13C2)PPh3Br. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance:(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is a colorless crystalline powder.
-Melting point: The melting point is higher, usually between 90-95°C.
-Solubility: It has good solubility in non-polar solvents, such as dimethylformamide and dichloromethane.
Use:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is often used as a reagent in organic synthesis. Its Main uses include the following aspects:
-As a phosphine bromide reagent: It can be used to introduce phosphate groups in organic synthesis.
-is a 13C isotope labeling reagent of phosphorus atom.
Preparation Method:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is generally prepared by the following steps:
1. Methyl acetate was added with methylene chloride labeled with carbon isotope (13C).
2. Add triphenylphosphonium bromide and base.
3. The reaction produces (CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE.
Please note that the preparation process involves organic synthesis reactions and needs to be carried out under appropriate conditions and necessary safety precautions.
Safety Information:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is a chemical reagent that should be properly disposed:
-Avoid contact with skin and eyes, such as contact should immediately rinse with plenty of water.
-Appropriate personal protective equipment, such as lab gloves and goggles, should be equipped during use.
-Store it tightly and away from oxidizers and flammables.
-Please follow the relevant safety operation procedures when using, and find the relevant safety data sheet to understand and follow the relevant safety operation guidelines in advance.
Nature:
-Appearance:(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is a colorless crystalline powder.
-Melting point: The melting point is higher, usually between 90-95°C.
-Solubility: It has good solubility in non-polar solvents, such as dimethylformamide and dichloromethane.
Use:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is often used as a reagent in organic synthesis. Its Main uses include the following aspects:
-As a phosphine bromide reagent: It can be used to introduce phosphate groups in organic synthesis.
-is a 13C isotope labeling reagent of phosphorus atom.
Preparation Method:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is generally prepared by the following steps:
1. Methyl acetate was added with methylene chloride labeled with carbon isotope (13C).
2. Add triphenylphosphonium bromide and base.
3. The reaction produces (CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE.
Please note that the preparation process involves organic synthesis reactions and needs to be carried out under appropriate conditions and necessary safety precautions.
Safety Information:
(CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE is a chemical reagent that should be properly disposed:
-Avoid contact with skin and eyes, such as contact should immediately rinse with plenty of water.
-Appropriate personal protective equipment, such as lab gloves and goggles, should be equipped during use.
-Store it tightly and away from oxidizers and flammables.
-Please follow the relevant safety operation procedures when using, and find the relevant safety data sheet to understand and follow the relevant safety operation guidelines in advance.
Last Update：2024-04-10 22:41:03
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Product Name: (CARBETHOXYMETHYL-1,2-13C2)TRIPHENYLPHOSPHONIUM BROMIDE Visit Supplier Webpage Request for quotation
CAS: 109376-35-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 109376-35-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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View History
[13C2]-Ethoxycarbonylmethyltriphenyl phosphonium Bromide
2-氯-1-环己基乙烷-1-酮
顺-5-十二碳烯-1-醇醋酸酯
2-Formyl-3-methylthiophene, 3-Methyl-2-thenaldehyde
1-Azabicyclo[2.2.2]octane-2-carboxylic acid, 3-oxo-, methyl ester
Fluoroclorgyline
1-Naphthalenecarboxylic acid, decahydro-4-oxo-, 5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl ester, [1S-[1α(1S*,2R*,5S*),4aβ,8aβ]]-
KINASE DOMAIN OF INSULIN RECEPTOR (2)
ANTI-OXPHOS COMPLEX IV SUBUNIT VIA-H, MOUSE IGG2A
Pyridine, 2,4-dimethyl-6-[(trimethylsilyl)methyl]-
2-氯-1-环己基乙烷-1-酮
顺-5-十二碳烯-1-醇醋酸酯
2-Formyl-3-methylthiophene, 3-Methyl-2-thenaldehyde
1-Azabicyclo[2.2.2]octane-2-carboxylic acid, 3-oxo-, methyl ester
Fluoroclorgyline
1-Naphthalenecarboxylic acid, decahydro-4-oxo-, 5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl ester, [1S-[1α(1S*,2R*,5S*),4aβ,8aβ]]-
KINASE DOMAIN OF INSULIN RECEPTOR (2)
ANTI-OXPHOS COMPLEX IV SUBUNIT VIA-H, MOUSE IGG2A
Pyridine, 2,4-dimethyl-6-[(trimethylsilyl)methyl]-