메틸렌트리페닐포스핀

Methylenetriphenylphosphorane

HCID 137960CAS 3487-44-3

기본 정보

표준 SMILES
C=P(c1ccccc1)(c1ccccc1)c1ccccc1
InChIKey
XYDYWTJEGDZLTH-UHFFFAOYSA-N
분자식
C19H17P
평균 분자량
276.3 g/mol
단동위원소 질량
276.10678717

이름 및 식별자

우선 이름
Methylenetriphenylphosphorane
IUPAC
methylidene(triphenyl)-λ5-phosphane
현지명
메틸렌트리페닐포스핀
영어명
Methylenetriphenylphosphine
분자식
C19H17P
분자량
276.31

이름 및 동의어

Methylenetriphenylphosphorane3487-44-3MethylenetriphenylphosphinePhosphorane, methylenetriphenyl-TriphenylmethylenephosphoraneTriphenylphosphomethyleneTriphenylphosphormethyleneTriphenylphosphine methyleneTriphenylphosphine methylideMethylidenetriphenylphosphoranemethylene(triphenyl)phosphoraneUNII-8GN8K95F62
이름 더 보기
메틸렌트리페닐포스핀SKL479RS RMA04960methylene-tri(phenyl)phosphoranemethylenetriphenyl - 15 - phosphanemethylidene-tri(phenyl)-$l^{5}-phosphane
8GN8K95F62DTXSID20188410METHYLENETRIPHENYLPHOSPHORANE [MI]RefChem:158206DTXCID50110901InChI=1/C19H17P/c1-20(17-11-5-2-6-12-17,18-13-7-3-8-14-18)19-15-9-4-10-16-19/h2-16H,1HXYDYWTJEGDZLTH-UHFFFAOYSA-NMethylenetriphenyl-l5-phosphane

데이터베이스 식별자

CAS
3487-44-3
PubChem CID
137960
DTXSID
DTXSID20188410
UNII
8GN8K95F62
Nikkaji
J109.666D、J785.103K

물성

구조 계산 물성

XLogP
4
극성 표면적
0 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
0
회전 가능 결합 수
3
무거운 원자 수
20

실험 및 물리화학적 성질

SpringerMaterials PropertiesChemical shift

물리화학적 성질

녹는점
96 °C · 96 °C
끓는 점
430 · 430.0±28.0 °C(Predicted)
밀도
1.1 · 1.10±0.1 g/cm3(Predicted)
용해도
sol ether, THF, DME, benzene, toluene, DMSO; water and protic solvents destroy the reagent completely
물리적 상태
yellow crystals turning white in air

안전 및 규제

안전 데이터

신호 어
Warning
유해·위험 문구
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드 H302

화학 및 산업

응용 분야

용도Methylenetriphenylphosphine is used as a methylenating agent for aldehydes and ketones; can convert lactols into hydroxy alkenes; can form a lithio derivative; can be transformed into a β-ketophosphorus ylide.

제조 방법 · 1건

Methylenetriphenylphosphine is usually prepared by treatment of a suspension of Methyltriphenylphosphonium Bromide (or iodide) in an appropriate solvent with a strong base. Butyllithium, dimsylsodium, t-BuOK, and sodamide are commonly used. Typically, a suspension of dry methyltriphenylphosphonium bromide in dry ether or THF is treated with n-Butyllithium at 0°C under N2 and the resulting solution is stirred at rt for 1 h. A yellow to deep orange color indicates the ylide formation. The dimsylsodium (Sodium Methylsulfinylmethylide) procedure requires heating a suspension of NaH in dry DMSO at 75-80 °C for 1 h followed by ice-cooling prior to the addition of phosphonium bromide. A salt-free ylide is usually prepared using Sodium Amide in liquid ammonia or in refluxing THF.

공급사7 곳

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