Cas 1101207-05-9,O-ethyl S-5-((4-fluorophenyl)(methyl)amino)-5-oxo-1-(propan-2-ylideneaminooxy)pentan-2-yl carbonodithioate

1101207-05-9

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Basic information

Product Name: O-ethyl S-5-((4-fluorophenyl)(methyl)amino)-5-oxo-1-(propan-2-ylideneaminooxy)pentan-2-yl carbonodithioate
Synonyms:
CAS NO:1101207-05-9
Molecular Formula:
Molecular Weight: 400.539
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: O-ethyl S-5-((4-fluorophenyl)(methyl)amino)-5-oxo-1-(propan-2-ylideneaminooxy)pentan-2-yl carbonodithioate(CAS DataBase Reference)
NIST Chemistry Reference: O-ethyl S-5-((4-fluorophenyl)(methyl)amino)-5-oxo-1-(propan-2-ylideneaminooxy)pentan-2-yl carbonodithioate(1101207-05-9)
EPA Substance Registry System: O-ethyl S-5-((4-fluorophenyl)(methyl)amino)-5-oxo-1-(propan-2-ylideneaminooxy)pentan-2-yl carbonodithioate(1101207-05-9)

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: 1101207-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101207-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,2,0 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1101207-05:
(9*1)+(8*1)+(7*0)+(6*1)+(5*2)+(4*0)+(3*7)+(2*0)+(1*5)=59
59 % 10 = 9
So 1101207-05-9 is a valid CAS Registry Number.

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1101207-05-9Relevant academic research and scientific papers

A versatile radical based approach to O-alkylated hydroxylamines and oximes

Quiclet-Sire, Béatrice,Woollaston, Daniel,Zard, Samir Z.

experimental part, p. 11917 - 11924 (2009/04/06)

O-Alkylhydroxylamines, often used for the preparation of bioconjugates, can be readily obtained by radical addition to suitable O-alkenylhydroxylamine derivatives. In the case of N-Boc-O-allylhydroxylamine, the addition is unexpectedly followed by elimination resulting in an overall allylation of the radical species.

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