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Merck
모든 사진(4)

주요 문서

431303

Sigma-Aldrich

Propylphosphonic anhydride solution

≥50 wt. % in ethyl acetate

동의어(들):

1-Propanephosphonic anhydride solution, 2,4,6-Tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide solution, PPACA, T3P®

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About This Item

실험식(Hill 표기법):
C9H21O6P3
CAS Number:
Molecular Weight:
318.18
Beilstein:
5079255
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

양식

liquid

Quality Level

농도

≥50 wt. % in ethyl acetate

refractive index

n20/D 1.418

bp

65 °C

density

1.069 g/mL at 25 °C

SMILES string

CCCP1(=O)OP(=O)(CCC)OP(=O)(CCC)O1

InChI

1S/C9H21O6P3/c1-4-7-16(10)13-17(11,8-5-2)15-18(12,14-16)9-6-3/h4-9H2,1-3H3

InChI key

PAQZWJGSJMLPMG-UHFFFAOYSA-N

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일반 설명

Propylphosphonic anhydride (T3P) is a reactive n-propyl phosphonic acid cyclic anhydride. It is a mild and low toxic coupling agent used in peptide synthesis. T3P also acts as a promoter and water scavenger in the Friedländer annulation reaction. It participates in the conversion of carboxylic acids and amides into nitriles, formation of Weinreb amides, ester synthesis, dehydrations, oxidation of alcohols, isonitrile synthesis, synthesis of alkenes from alcohols and C-C coupling reactions. T3P delivers outstanding advantages over traditional reagents, such as broad functional group tolerance, low epimerization, and water-soluble by-products and hence gives high purity and yield of the product.

애플리케이션

Propylphosphonic anhydride (T3P) can be used:
  • As an acid-amine coupling reagent for the synthesis of 3-(trifluoromethyl)-1H-pyrazole-5-carboxamides which are potent activators of pyruvate kinase M2 (PKM2).
  • In the synthesis of substituted benzofurans as potent DNA gyraseB inhibitors of Mycobacterium tuberculosis.
  • As a catalyst in the synthesis of benzothiazoles, benzoxazoles, and benzimidazoles under microwave irradiation.
  • As a catalyst in the conversion of ketoximes to amides and aldoximes to nitriles via Beckmann rearrangement.
  • As a reagent in the one-pot conversion of aromatic, heteroaromatic, and aliphatic aldehydes to nitriles.
Propylphosphonic anhydride may be used in the following studies:
  • As coupling agent for the synthesis of bispyridine-based ligands, which are used as bridging linkers in multinuclear platinum anticancer drugs.
  • Microwave-assissted Fischer indolization of arylhydrazines.
  • As acid activating agent for the direct synthesis of acid azides from carboxylic acids.
  • One-pot synthesis of coumarins.
  • Microwave-mediated synthesis of carbocyclic and heterocyclic fused quinolones.
  • One-pot synthesis of 1,2,4-oxadiazoles, 1,3,4-oxadiazoles, and 1,3,4-thiadiazoles from carboxylic acids.
  • Activation of the carboxyl group for hydroxyamidation and peptide coupling and in the one-pot conversion of carboxylic acids into hydroxamic acids.

법적 정보

T3P is a registered trademark of Archimica GmbH

관련 제품

제품 번호
설명
가격

픽토그램

FlameCorrosionExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

표적 기관

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

24.8 °F - closed cup

Flash Point (°C)

-4 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles


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문서 라이브러리 방문

Glauder, J.
Spec. Chem., 24(3), 30-30 (2004)
A microwave-assisted, propylphosphonic anhydride (T3P?) mediated one-pot Fischer indole synthesis.
Desroses M, et al.
Tetrahedron Letters, 52(34), 4417-4420 (2011)
An efficient catalytic method for the Beckmann rearrangement of ketoximes to amides and aldoximes to nitriles mediated by propylphosphonic anhydride (T3P)
Augustine JK, et al.
Tetrahedron Letters, 52(10), 1074-1077 (2011)
T3P: A convenient and useful reagent in organic synthesis
Garcia Ariel LL, et al.
Synlett, 2007(08), 1328-1329 (2007)
Design, synthesis, biological evaluation of substituted benzofurans as DNA gyraseB inhibitors of Mycobacterium tuberculosis
Renuka J, et al.
Bioorganic & Medicinal Chemistry, 22(17), 4924-4934 (2014)

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