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(Methoxymethyl)triphenylphosphonium chloride

(Methoxymethyl)triphenylphosphonium chloride structure

(Methoxymethyl)triphenylphosphonium chloride 

structure
  • CAS No:

    4009-98-7

  • Formula:

    C20H20OP.Cl

  • Chemical Name:

    (Methoxymethyl)triphenylphosphonium chloride

  • Synonyms:

    Phosphonium,(methoxymethyl)triphenyl-,chloride (1:1);Phosphonium,(methoxymethyl)triphenyl-,chloride;(Methoxymethyl)triphenylphosphonium chloride;Triphenyl(methoxymethyl)phosphonium chloride;NSC 49223;[(Methyloxy)methyl]triphenylphosphonium chloride;(Methoxymethyl)triphenylphosphanium chloride;130927-82-1;733747-55-2;1401904-62-8;2376192-44-6

  • Categories:

    Pharmaceutical Intermediates  >  Antineoplastics

Description

WHITE TO ALMOST WHITE FINE CRYSTALLINE POWDER

(Methoxymethyl)triphenylphosphonium chloride Basic Attributes

342.8

342.094025

924215

223-664-5

49223

29310095

Characteristics

9.2

0.58840

White to almost white Crystalline Powder

191-193 °C

>250°C

Decomposes in water

2-8°C

Safety Information

UN 1390 4.3/PG 2

3

22-36/37/38

26-36-24/25

Xn,Xi

Harmful

Stable at room temperature in closed containers under normal storage and handling conditions. Hygroscopic: absorbs moisture or water from the air.

P261-P305 + P351 + P338

H302-H315-H319-H335

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 52 companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

(Methoxymethyl)triphenylphosphonium chloride Use and Manufacturing

Methods of Manufacturing

20 g of triphenylphosphine was placed in a round bottom flask, dissolved in toluene, heated to 95 ° C, and 6.37 mL of chloromethyl methyl ether was added, and the reaction was carried out for 16 hours. After the reaction is complete, Cool to room temperature, filter, filter cake washed with toluene three times, dry, Obtained 25.4 g of white phosphonium salt, yield 97.3percentUnder nitrogen, 50 mL of anhydrous acetone was added to the reactor, Then 32 g of triphenylphosphine was added, While stirring, the temperature was raised to 37 ° C, While maintaining the temperature, 20 g of methyl chloromethyl ether was added to the reactor, Followed by reaction at 37 ° C for 3 h, The temperature was gradually raised to 47 ° C at a rate of 1 ° C / min and the reaction was continued for 3 h, The reaction was stopped, filtered, washed with anhydrous ether, dried, To give 37.0 g (methoxymethyl) triphenylphosphonium chloride in a yield of 88.5percent.

Uses

PTC catalyst Intermediates of Liquid Crystals

Computed Properties

Molecular Weight:342.8
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:342.0940299
Monoisotopic Mass:342.0940299
Topological Polar Surface Area:9.2
Heavy Atom Count:23
Complexity:266
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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