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Morpholine, 4-[1-(4,5-dimethyl-2-oxido-1,3,2-dioxaphospholan-2-yl)-1-phenylethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136001-39-3

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136001-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136001-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,0,0 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136001-39:
(8*1)+(7*3)+(6*6)+(5*0)+(4*0)+(3*1)+(2*3)+(1*9)=83
83 % 10 = 3
So 136001-39-3 is a valid CAS Registry Number.

136001-39-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[1-(4,5-Dimethyl-2-oxo-2λ5-[1,3,2]dioxaphospholan-2-yl)-1-phenyl-ethyl]-morpholine

1.2 Other means of identification

Product number -
Other names -

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:136001-39-3 SDS

136001-39-3Downstream Products

136001-39-3Relevant academic research and scientific papers

Thermochemical characteristics of phosphorous acid derivatives

Sagdeev,Safina

, p. 248 - 252 (2007/12/31)

Enthalpies of formation enthalpies of a series of phosphorous acid derivatives were estimated from the heat effects of their reactions. The collected thermochemical data was used to analyze, on the basis of the additive scheme, the experimental enthalpies

Thermochemistry and Kinetics of the Electrophilic Pudovik Reaction

Ovchinnikov

, p. 449 - 452 (2007/10/03)

The thermochemistry and kinetics of five- and six-membered cyclic and acyclic phosphonates in the AdE Pudovik reaction with substituted morpholinoethenes was studied. The high activity of the phospholane derivative in this process to a consider

SOME KINETIC LAWS AND THE MECHANISM OF REACTIONS OF INCOMPLETE ESTERS OF PHOSPHOROUS ACID WITH ENAMINES

Safina, Yu. G.,Malkova, G. Sh.,Cherkasov, R. A.

, p. 1275 - 1283 (2007/10/02)

A kinetic study of reactions of cyclic and acyclic incomplete esters of phosphorous acid with enamines, enaminoesters, and enaminoketones was conducted by a spectrophotometric method.With derivatives of 1-morpholino-1-phenylethene substituted in the para position of the benzene ring the reaction proceeds in two steps according to an AdE scheme with the phosphorous component of electronic factors exerting the deciding influence on reactivity.The rate-determining step of the addition of acid phosphites to enamines is nucleophilic addition of phosphite at the C=C bond within the H complex of the enaminone with the acid according to a monomolecular mechanism.

REACTION OF CYCLIC PARTIAL PHOSPHITE ESTERS WITH ENAMINES - AN ELECTROPHILIC FORM OF THE PUDOVIK REACTION

Safina, Yu. G.,Malkova, G. Sh.,Cherkasov, R. A.

, p. 562 - 574 (2007/10/02)

It was established that the ease of noncatalytic addition of cyclic and acyclic partial phosphites to enamines is due to the H-donor capacity of the acids and to the degree of localization of the electron density at the C=C bond in the unsaturated partner.It was shown that cyclic phosphites add initially at the carbon-carbon multiple bond of the conjugated N-C=C-C=O system of enamino ketones with the final formation of bisphosphorylated derivatives.

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