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1017-88-5

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1017-88-5 Usage

General Description

DIMETHYLDIPHENYLPHOSPHONIUM IODIDE is a chemical compound with the molecular formula C14H16IP. It is an ionic compound consisting of a phosphonium cation and an iodide anion. DIMETHYLDIPHENYLPHOSPHONIUM IODIDE is commonly used as a reagent in organic synthesis, especially in the preparation of Wittig reagents for olefin synthesis. It is also used in the pharmaceutical industry as a precursor for the synthesis of various pharmaceutical drugs. DIMETHYLDIPHENYLPHOSPHONIUM IODIDE is a white crystalline solid that is soluble in organic solvents and is commonly handled and stored in a moisture-free environment due to its sensitivity to moisture.

Check Digit Verification of cas no

The CAS Registry Mumber 1017-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1017-88:
(6*1)+(5*0)+(4*1)+(3*7)+(2*8)+(1*8)=55
55 % 10 = 5
So 1017-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H16P/c1-15(2,13-9-5-3-6-10-13)14-11-7-4-8-12-14/h3-12H,1-2H3/q+1

1017-88-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl(diphenyl)phosphanium,iodide

1.2 Other means of identification

Product number -
Other names Dimethyl-diphenyl-phosphonium,Jodid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1017-88-5 SDS

1017-88-5Relevant articles and documents

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Gans,P.,Smith,B.C.

, p. 4172 - 4176 (1964)

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The absolute configuration of isochamigrene: New insights into the cyclisation mechanism of trichodiene synthase

Burkhardt, Immo,Dickschat, Jeroen S.

, p. 3540 - 3542 (2018)

Isochamigrene, a side product of the trichodiene synthase, which is a key enzyme from the biosynthesis of the trichothecene mycotoxins from Fusarium spp., was enantioselectively synthesised and compared to the natural product from Fusarium sporotrichioides. As a result, its absolute configuration was assigned to (S)-isochamigrene. Implications for the recently extensively discussed cyclisation mechanism towards trichodiene and its side products are discussed.

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Johnson et al.

, p. 1338,1343 (1965)

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Design and Synthesis of the Active Site Environment in Zeolite Catalysts for Selectively Manipulating Mechanistic Pathways

Li, Chengeng,Ferri, Pau,Paris, Cecilia,Moliner, Manuel,Boronat, Mercedes,Corma, Avelino

supporting information, p. 10718 - 10726 (2021/07/28)

By combining kinetics and theoretical calculations, we show here the benefits of going beyond the concept of static localized and defined active sites on solid catalysts, into a system that globally and dynamically considers the active site located in an

ITQ-40, New Crystalline Microporous Material

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Page/Page column 6, (2011/07/08)

ITQ-40 (INSTITUTO DE TECNOLOGíA QUíMICA number 40) is a new crystalline microporous material with a framework of tetrahedral atoms connected by atoms capable of bridging the tetrahedral atoms, the tetrahedral atom framework being defined by the interconne

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