Cas 16276-74-7,MORPHOLIN-4-YLPHOSPHONOCHLORIDOUS ACID METHYLESTER

16276-74-7

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Basic information

Product Name: MORPHOLIN-4-YLPHOSPHONOCHLORIDOUS ACID METHYLESTER
Synonyms: Ethyl morpholin-4-ylphosphonochloridoite; Phosphonochloridous acid, P-4-morpholinyl-, ethyl ester
CAS NO:16276-74-7
Molecular Formula: C6H13ClNO2P
Molecular Weight: 197.6
EINECS: N/A
Product Categories: N/A
Mol File: 16276-74-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 237.9°C at 760 mmHg
Flash Point: 97.7°C
Appearance: /
Density: N/A
Vapor Pressure: 0.0438mmHg at 25°C
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
PKA: -1.37±0.20(Predicted)
CAS DataBase Reference: MORPHOLIN-4-YLPHOSPHONOCHLORIDOUS ACID METHYLESTER(CAS DataBase Reference)
NIST Chemistry Reference: MORPHOLIN-4-YLPHOSPHONOCHLORIDOUS ACID METHYLESTER(16276-74-7)
EPA Substance Registry System: MORPHOLIN-4-YLPHOSPHONOCHLORIDOUS ACID METHYLESTER(16276-74-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 16276-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 16276-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16276-74:
(7*1)+(6*6)+(5*2)+(4*7)+(3*6)+(2*7)+(1*4)=117
117 % 10 = 7
So 16276-74-7 is a valid CAS Registry Number.

InChI:InChI=1/C6H13ClNO2P/c1-2-10-11(7)8-3-5-9-6-4-8/h2-6H2,1H3

16276-74-7Upstream product

16276-74-7Downstream Products

16276-74-7Relevant academic research and scientific papers

AMIDATION OF HALOGEN DERIVATIVES OF PHOSPHORUS WITH 4,4',4''-METHYLIDYNETRISMORPHOLINE

Shevchenko, M. V.,Kukhar', V. P.

, p. 1336 - 1340 (2007/10/02)

4,4'4''-Methylidynetrismorpholine amidates polyhalophosphorus compounds and is a more reactive agent than the previously studied N,N,N'N'-tetraalkylmethanediamines.The dimorpholinomethylium chloride formed as a result of the reaction does not react with the amidation products, which makes it possible to isolate them in a pure state.

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