Cas 1101207-02-6,S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate

1101207-02-6

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Basic information

Product Name: S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate
Synonyms: S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate
CAS NO:1101207-02-6
Molecular Formula:
Molecular Weight: 484.468
EINECS: N/A
Product Categories: N/A
Mol File: 1101207-02-6.mol
Article Data: 1

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: S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate(CAS DataBase Reference)
NIST Chemistry Reference: S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate(1101207-02-6)
EPA Substance Registry System: S-1-((bis(4-chlorophenyl)methylene)aminooxy)-5-oxohexan-2-yl O-ethyl carbonodithioate(1101207-02-6)

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: 1101207-02-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101207-02-6 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 1101207-02:
(9*1)+(8*1)+(7*0)+(6*1)+(5*2)+(4*0)+(3*7)+(2*0)+(1*2)=56
56 % 10 = 6
So 1101207-02-6 is a valid CAS Registry Number.

1101207-02-6Upstream product

1101207-02-6Downstream Products

1101207-18-4 6-((bis(4-chlorophenyl)methylene)aminooxy)hexan-2-one

1101207-02-6Relevant articles and documents

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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