CAS 1530-45-6

Phosphonium, (2-ethoxy-2-oxoethyl)triphenyl-, bromide (1:1)

Description:

Phosphonium, (2-ethoxy-2-oxoethyl)triphenyl-, bromide (1:1), with the CAS number 1530-45-6, is a quaternary ammonium compound characterized by a positively charged phosphonium ion and a bromide counterion. This substance typically exhibits properties associated with phosphonium salts, such as high thermal stability and solubility in organic solvents. The presence of the triphenyl group contributes to its lipophilicity, making it useful in various organic synthesis applications. The ethoxy and keto functionalities suggest potential reactivity, allowing it to participate in nucleophilic substitution reactions or serve as a catalyst in organic transformations. Additionally, the bromide ion can act as a leaving group in chemical reactions. Overall, this compound is of interest in fields such as organic chemistry and materials science, where it may be utilized in the development of new synthetic methodologies or as an intermediate in the production of more complex molecules.

Formula: C₂₂H₂₂O₂P·Br

InChI: InChI=1S/C22H22O2P.BrH/c1-2-24-22(23)18-25(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21;/h3-17H,2,18H2,1H3;1H/q+1;/p-1

InChI key: InChIKey=VJVZPTPOYCJFNI-UHFFFAOYSA-M

SMILES: [P+](CC(OCC)=O)(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.[Br-]

Synonyms:

• (2-Ethoxy-2-Oxoethyl)(Triphenyl)Phosphonium
• (2-Ethoxy-2-Oxoethyl)(Triphenyl)Phosphonium Bromide
• (Carboethoxymethyl)triphenylphosphonium bromide
• (Carboxymethyl)triphenylphosphonium bromide ethyl ester
• (Ethoxycarbonylmethyl)triphenylphosphonium bromide
• Carbethoxy Methyl Triphenyl Phosphonium Bromide
• Carboethoxymethyltriphenylphosphonium bromide
• Cemtppb
• Ethoxycarbonylmethyltriphenylphosphonium bromide
• Ethyl (triphenylphosphonio)acetate bromide
• NSC 60450
• Phosphonium, (2-ethoxy-2-oxoethyl)triphenyl-, bromide
• Phosphonium, (2-ethoxy-2-oxoethyl)triphenyl-, bromide (1:1)
• Phosphonium, (carboxymethyl)triphenyl-, bromide, ethyl ester
• (Carbethoxymethyl)triphenylphosphonium bromide

Ethoxycarbonylmethyl(triphenyl)phosphonium Bromide

CAS: 1530-45-6

Formula: C₂₂H₂₂BrO₂P

Purity: >97.0%(T)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 429.29

Ref: 3B-E0407

(Ethoxycarbonylmethyl)triphenylphosphonium bromide, 98+%

CAS: 1530-45-6

(Ethoxycarbonylmethyl)triphenylphosphonium bromide, is used as a pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar produc

Formula: C₂₂H₂₂BrO₂P

Purity: 98+%

Color and Shape: White to cream, Powder or crystalline powder

Molecular weight: 429.29

Ref: 02-A16347

(2-Ethoxy-2-oxoethyl)triphenylphosphonium bromide

CAS: 1530-45-6

Formula: C₂₂H₂₂BrO₂P

Purity: 98%

Color and Shape: Solid

Molecular weight: 429.2866

Ref: IN-DA0032D7

Carbethoxymethyltriphenylphosphonium bromide

CAS: 1530-45-6

Formula: CH₃CH₂O₂CCH₂P(C₆H₅)₃Br

Molecular weight: 429.30

Ref: 7W-GK7830

(Ethoxycarbonylmethyl)triphenylphosphonium bromide

CAS: 1530-45-6

(Ethoxycarbonylmethyl)triphenylphosphonium bromide

Formula: C₂₂H₂₂O₂P·Br

Purity: 98%

Color and Shape: white powder

Molecular weight: 429.29g/mol

Ref: 54-OR10646

Ethoxycarbonylmethyl-triphenyl-phosphonium bromide

CAS: 1530-45-6

Formula: C₂₂H₂₂BrO₂P

Purity: 98%

Color and Shape: Solid, White - Slightly pale reddish yellow powder

Molecular weight: 429.294

Ref: 10-F049919

(Ethoxycarbonylmethyl)triphenylphosphonium-13C2d2 Bromide

Controlled Product

CAS: 1530-45-6, 793628-37-2

Formula: C₂C₂₀D₂H₁₉O₂P·Br

Color and Shape: Neat

Molecular weight: 432.276

Ref: TR-E891451

(Ethoxycarbonylmethyl)triphenylphosphonium Bromide

Controlled Product

CAS: 1530-45-6

Applications (Ethoxycarbonylmethyl)triphenylphosphonium bromide is an intermediate in the synthesis of 3-Chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone-13C5, which is an isotope labelled Mutagen X (MX) is a chlorinated furanone that accounts for more of the mutagenic activity of drinking water than any other disinfection byproduct. DNA damages provoked by the six mutagens (furylframide, MX, 4-nitroquinoline N-oxide, sodium azide, 1-nitropyrene, and captan) used in the present study have been known to subject to the nucleotide excision repair system.
References Hakulinen, P., et al.: Toxicol. Lett., 151, 439 (2004), Richardson, S., et al.: Mutat. Res., 636, 178 (2007), Kim, J., et al.: Environ. Toxicol., 23, 319 (2008),

Formula: C₂₂H₂₂BrO₂P

Color and Shape: Neat

Molecular weight: 429.29

Ref: TR-E891450