(2-Nitrobenzyl)triphenylphosphonium Brmide

(2-Nitrobenzyl)triphenylphosphonium Brmide - Names and Identifiers

Name	(2-Nitrobenzyl)triphenylphosphonium bromide monohydrate
Synonyms	Nsc226219 (2-nitrobenzyl)(triphenyl)phosphonium (2-Nitrobenzyl)triphenylphosphonium Brmide (2-NITROBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE (2-NITROBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE HYDRATE (2-NITROBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE MONOHYDRATE (2-Nitrobenzyl)triphenylphosphonium bromide monohydrate (2-NITROBENZYL)TRIPHENYLPHOSPHONIUM BROMIDE MONOHYDRATE, 98+
CAS	23308-83-0
InChI	InChI=1/C25H21NO2P.BrH.H2O/c27-26(28)25-19-11-10-12-21(25)20-29(22-13-4-1-5-14-22,23-15-6-2-7-16-23)24-17-8-3-9-18-24;;/h1-19H,20H2;1H;1H2/q+1;;/p-1

(2-Nitrobenzyl)triphenylphosphonium Brmide - Physico-chemical Properties

Molecular Formula	C25H21BrNO2P
Molar Mass	478.33
Melting Point	238-240°C
BRN	4086172
Storage Condition	2-8℃
MDL	MFCD04971966

(2-Nitrobenzyl)triphenylphosphonium Brmide - Risk and Safety

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.

(2-Nitrobenzyl)triphenylphosphonium Brmide - Introduction

(2-Nitrobenzyl) triphenylphosphonium bromide, monohydrate is an organic compound with the chemical formula C27H22BrNO3P · H2O. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance: White crystalline solid
-Melting Point: 220-222 ℃
-Solubility: Soluble in ethanol, chloroform and Ether solvents

Use:
(2-Nitrobenzyl) triphenylphosphonium bromide is commonly used as a reagent in organic synthesis. It can function as a catalyst or reagent in a variety of reactions, such as alkylation and substitution reactions in organic synthesis.

Method:
(2-Nitrobenzyl) triphenylphosphine bromide can be synthesized by different methods, depending on the desired target product and the availability of the starting material. Common synthetic methods include the reaction of benzylmagnesium bromide with triphenylphosphine, and the acid-catalyzed reaction of p-nitrobenzyl alcohol with hydrogen bromide.

Safety Information:
-The compound should be handled and stored to avoid contact with skin and eyes.
-Wear appropriate protective equipment, such as gloves, glasses and lab coats.
-Avoid inhaling its powder during operation.
-Waste should be disposed of in accordance with local regulations.

Last Update：2024-04-10 22:29:15