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137334-99-7

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137334-99-7 Usage

Reactivity

Highly reactive

Versatility

Versatile reagent

Applications

Chemical synthesis, catalysis

Character

Strong nucleophilic character

Substrate activation

Ability to activate a wide range of substrates

Value

Valuable tool in organic synthesis

Development

Used in the development of new methodologies for the synthesis of complex molecules

Preparation

Used in the preparation of pharmaceutical compounds

Importance

Powerful and important chemical reagent

Research and industry

Various potential applications in chemical research and industry

Check Digit Verification of cas no

The CAS Registry Mumber 137334-99-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,3,3 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137334-99:
(8*1)+(7*3)+(6*7)+(5*3)+(4*3)+(3*4)+(2*9)+(1*9)=137
137 % 10 = 7
So 137334-99-7 is a valid CAS Registry Number.

137334-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(dimethylamino)-[[tris(dimethylamino)-λ<sup>5</sup>-phosphanylidene]amino]phosphanium,fluoride

1.2 Other means of identification

Product number -
Other names Phosphazenebase P2-F

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:137334-99-7 SDS

137334-99-7Upstream product

137334-99-7Downstream Products

137334-99-7Relevant articles and documents

Heavy silylchalcogenido lanthanates synthesis Ph4P[Cp3La-ESiMe3] (E = S, Se, and Te): Via fluoride-induced demethylation of dimethylcarbonate to Ph4P[OCO2Me] key intermediate

Guschlbauer, Jannick,Vollgraff, Tobias,Xie, Xiulan,Fetoh, Ahmed,Sundermeyer, J?rg

supporting information, p. 13103 - 13111 (2021/10/12)

We report a new high-yield synthesis of so far not accessible tetraphenylphosphonium methylcarbonate Ph4P[OCO2Me] via solvothermal fluoride-induced demethylation and MeF elimination at Me2CO3 (DMC) by Ph4P-F, structurally characterized as λ5-fluorophospho

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