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Colorless liquid with a characteristic odor

20195-08-8

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20195-08-8 Usage

Type of compound

Organophosphate ester

Primary use

Solvent in various industrial applications

Secondary use

Organic synthesis and as a reagent in chemical reactions

Volatility

Low

Water solubility

Low

Handling precautions

Handle with care, use in well-ventilated area with proper personal protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 20195-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,9 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20195-08:
(7*2)+(6*0)+(5*1)+(4*9)+(3*5)+(2*0)+(1*8)=78
78 % 10 = 8
So 20195-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H21O4P/c1-4-7-8-9-13-14(10,11-5-2)12-6-3/h4-9H2,1-3H3

20195-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl pentyl phosphate

1.2 Other means of identification

Product number -
Other names 1-DIETHOXYPHOSPHORYLOXYPENTANE

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:20195-08-8 SDS

20195-08-8Downstream Products

20195-08-8Relevant academic research and scientific papers

Cross-hetero-dehydrogenative coupling reaction of phosphites: A catalytic metal-free phosphorylation of amines and alcohols

Dhineshkumar, Jayaraman,Prabhu, Kandikere Ramaiah

supporting information, p. 6062 - 6065 (2014/01/06)

Phosphorylation of amines, alcohols, and sulfoximines are accomplished using molecular iodine as a catalyst and H2O2 as the sole oxidant under mild reaction conditions. This method provides an easy route for synthesizing a variety of phosphoramidates, phosphorus triesters and sulfoximine-derived phosphoramidates which are of biological importance.

Synthesis of mixed alkylphosphites and alkylphosphates

Ilia, Gheorghe,Popa, Adriana,Iliescu, Smaranda,Bora, Alina,Dehelean, Gheorghe,Pascariu, Aurelia

, p. 1513 - 1519 (2007/10/03)

Some mixed phosphites having two different alkyl chain were obtained as forerunners for mixed phosphates Mixed dialkyl phosphates were obtained in good yields (40-80%) by phase transfer catalysis in liquid-liquid sistem, starting from different dialkyl phosphites and aliphatic alcohols. The reaction conditions were optimized in order to obtain good yields in phosphites and phosphates respectively. Compounds were analyzed by IR, P31-NMR.

Direct Esterification of Phosphates with Various Halides and its Application to Synthesis of cAMP Alkyl Triesters

Furuta, Toshiaki,Torigai, Hiromi,Osawa, Tomoko,Iwamura, Michiko

, p. 3139 - 3142 (2007/10/02)

Esterification of phosphates with various halides, including acid chlorides, phosphoryl trichloride and chloride, was achieved in 57-99percent isolated yield using silver(I) oxide.The reaction was successfully applied to the preparation of phosphate triesters sensitive to acids and bases. cAMP benzyl esters were also prepared by this method.

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