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37097-43-1

37097-43-1

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37097-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37097-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,0,9 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 37097-43:
(7*3)+(6*7)+(5*0)+(4*9)+(3*7)+(2*4)+(1*3)=131
131 % 10 = 1
So 37097-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H18NO4P/c1-3-12-14(10,13-4-2)9-5-7-11-8-6-9/h3-8H2,1-2H3

37097-43-1SDS

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-Diethoxyphosphorylmorpholine

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:37097-43-1 SDS

37097-43-1Downstream Products

37097-43-1Relevant articles and documents

Phosphoramidate synthesis via copper-catalysed aerobic oxidative coupling of amines and H-phosphonates

Fraser, Jamie,Wilson, Laura J.,Blundell, Rebecca K.,Hayes, Christopher J.

supporting information, p. 8919 - 8921 (2013/09/24)

The copper-catalysed oxidative coupling of amines and H-phosphonates to produce phosphoramidates has been achieved using CuI as the catalyst and O 2 (present in air) as the sole oxidant.

REACTIONS OF 4-MORPHOLINESULFENYL CHLORIDE WITH TRIALKYL PHOSPHITES

Mazitova, F. N.,Kharullin, V. K.

, p. 694 - 695 (2007/10/02)

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SOLVOLYSIS OF DIPHENYL AMIDOPHOSPHATES IN AQUEOUS ALCOHOLIC MEDIA

Kasparek, Frantisek,Mollin, Jiri

, p. 386 - 396 (2007/10/02)

Influence of substituent on the reaction rate of the alkali-catalyzed solvolysis of the studied compounds set has been followed.The activation entropy has also been determined.The reaction products have been identified, and their concentration ratio has been determined.The reaction selectivity is mostly influenced by sterical effects in the substrate molecule.The results obtained agree with the SN2 mechanism.

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