Cas 920526-13-2,Phosphorochloridamidic acid, N-(phenylmethyl)-N-2-propen-1-yl-, phenyl ester

920526-13-2

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Basic information

Product Name: Phosphorochloridamidic acid, N-(phenylmethyl)-N-2-propen-1-yl-, phenyl ester
Synonyms:
CAS NO:920526-13-2
Molecular Formula: C16H17ClNO2P
Molecular Weight: 321.743
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Phosphorochloridamidic acid, N-(phenylmethyl)-N-2-propen-1-yl-, phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Phosphorochloridamidic acid, N-(phenylmethyl)-N-2-propen-1-yl-, phenyl ester(920526-13-2)
EPA Substance Registry System: Phosphorochloridamidic acid, N-(phenylmethyl)-N-2-propen-1-yl-, phenyl ester(920526-13-2)

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: 920526-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 920526-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,0,5,2 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 920526-13:
(8*9)+(7*2)+(6*0)+(5*5)+(4*2)+(3*6)+(2*1)+(1*3)=142
142 % 10 = 2
So 920526-13-2 is a valid CAS Registry Number.

920526-13-2Upstream product

920526-13-2Downstream Products

920526-15-4 phenyl 1-phenylvinyl allyl(benzyl)phosphonamidate

920526-13-2Relevant academic research and scientific papers

Metathesis studies to cyclic enol phosphonamidates

Sieck, Stephen R.,McReynolds, Matthew D.,Schroeder, Chad E.,Hanson, Paul R.

, p. 5307 - 5311 (2007/10/03)

The development of cyclic, six membered enol phosphonamidates utilizing the ring-closing metathesis (RCM) reaction is discussed. Phosphonamidic monochloridates are generated and further functionalized to an array of acyclic, enol phosphonamidates. Subsequ

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