모든 사진(1)
About This Item
Linear Formula:
(CH3)3P
CAS Number:
Molecular Weight:
76.08
Beilstein:
969138
MDL number:
UNSPSC 코드:
12352128
PubChem Substance ID:
NACRES:
NA.22
추천 제품
양식
liquid
Quality Level
반응 적합성
reagent type: ligand
reaction type: Mitsunobu Reaction
reagent type: ligand
reaction type: Wittig Reaction
농도
1.0 M in THF
density
0.872 g/mL at 25 °C
작용기
phosphine
SMILES string
CP(C)C
InChI
1S/C3H9P/c1-4(2)3/h1-3H3
InChI key
YWWDBCBWQNCYNR-UHFFFAOYSA-N
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관련 카테고리
일반 설명
Trimethylphosphine is the reagent used in Mitsunobu reaction. It participates in the transformation of azides into carbamates, aziridines from azidoalcohols, iminophosphoranes and aza-Wittig reaction. Electron diffraction study of trimethylphosphine has been reported.
애플리케이션
Trimethylphosphine (PMe3) solution is the suitable reagent used in the synthesis of Fe/Te cluster type complex, Fe6Te8(PMe3)6. It may be employed as a probe to investigate the acid sites in Y-zeolite. It may be used for the synthesis of hexakis(trimethylphosphine)tris-μ-methylene-diruthenium(III).
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Central nervous system, Respiratory system
보충제 위험성
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
-22.0 °F - closed cup
Flash Point (°C)
-30 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Acid sites in zeolite Y: a solid-state NMR and infrared study using trimethylphosphine as a probe molecule.
Lunsford JH, et al.
Journal of the American Chemical Society, 107(6), 1540-1547 (1985)
Synthesis and x-ray crystal structures of hexakis (trimethylphosphine) tris-. mu.-methylene-diruthenium (III) and its mono-and dicationic derivatives.
Hursthouse MB, et al.
Journal of the American Chemical Society, 101(15), 4128-4139 (1979)
Effect of Diverse Ligands on the Course of a Molecules-to-Solids Process and Properties of Its Intermediates.
Steigerwald ML, et al.
Inorganic Chemistry, 33(15), 3389-3395 (1994)
Electron diffraction study of the structure of trimethylphosphine.
Bartell LS and Brockway LO.
J. Chem. Phys. , 32(2), 512-515 (1960)
N C Goomer et al.
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 19(6), 679-684 (1992-08-01)
Tc-99m monocationic mixed ligand complexes of phenyl substituted/condensed Schiff's bases, N,N'-ethylene-bis-(benzoylacetone imine) (Lb) or N,N'-ethylene-bis-(salicylaldehyde imine) (Lc) or N,N'-ethylene-bis-(2-hydroxyacetophenone imine) (Ld) and trimethylphosphine were synthesized to determine the influence of the presence of a phenyl group in these tracers on
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