309567
(Methoxymethyl)triphenylphosphonium chloride
97%
동의어(들):
Triphenyl(methoxymethyl)phosphonium chloride
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모든 사진(1)
About This Item
Linear Formula:
(C6H5)3P(Cl)CH2OCH3
CAS Number:
Molecular Weight:
342.80
Beilstein:
3599844
EC Number:
MDL number:
UNSPSC 코드:
12352107
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
solid
반응 적합성
reaction type: C-C Bond Formation
mp
185-195 °C (dec.) (lit.)
작용기
ether
phosphine
SMILES string
[Cl-].COC[P+](c1ccccc1)(c2ccccc2)c3ccccc3
InChI
1S/C20H20OP.ClH/c1-21-17-22(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20;/h2-16H,17H2,1H3;1H/q+1;/p-1
InChI key
SJFNDMHZXCUXSA-UHFFFAOYSA-M
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애플리케이션
(Methoxymethyl)triphenylphosphonium chloride is a Wittig reagent that reacts with aldehydes and ketones to give substituted alkenes. This Wittig reaction finds application as the key step in the synthesis of:
- Antimalarial drug, (+)-artemisinin.
- Substituted quinolines.
- Akuammiline alkaloid picrinine.
- 7H-pyrrolo[2,3-d]pyrimidine derivatives for signal transducers and activators of transcription 6 (STAT6) inhibitors.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
>482.0 °F
Flash Point (°C)
> 250 °C
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
Total synthesis of the akuammiline alkaloid picrinine
Smith JM, et al.
Journal of the American Chemical Society, 136(12), 4504-4507 (2014)
Novel 7H-pyrrolo [2, 3-d] pyrimidine derivatives as potent and orally active STAT6 inhibitors
Nagashima S, et al.
Bioorganic & Medicinal Chemistry, 17(19), 6926-6936 (2009)
Stereoselective total synthesis of (+)-artemisinin
Yadav JS, et al.
Tetrahedron Letters, 44(2), 387-389 (2003)
A convenient synthesis of quinolines by reactions of o-isocyano-β-methoxystyrenes with nucleophiles
Kobayashi K, et al.
Tetrahedron, 60(50), 11639-11645 (2004)
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