Cas 110840-36-3,1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester

110840-36-3

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Basic information

Product Name: 1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester
Synonyms: 1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester
CAS NO:110840-36-3
Molecular Formula:
Molecular Weight: 317.335
EINECS: N/A
Product Categories: N/A
Mol File: 110840-36-3.mol
Article Data: 2

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: 1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester(110840-36-3)
EPA Substance Registry System: 1-Difluoromethyl-3,3-diphenyl-aziridine-2-carboxylic acid ethyl ester(110840-36-3)

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: 110840-36-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110840-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,8,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110840-36:
(8*1)+(7*1)+(6*0)+(5*8)+(4*4)+(3*0)+(2*3)+(1*6)=83
83 % 10 = 3
So 110840-36-3 is a valid CAS Registry Number.

110840-36-3Upstream product

110840-36-3Downstream Products

110840-36-3Relevant articles and documents

Unprecedented 1,3-dipolar cycloaddition of azomethine ylides derived from difluorocarbene and imines to carbonyl compounds. - Synthesis of oxazolidine derivatives

Novikov, Mikhail S.,Khlebnikov, Alexander F.,Krebs, Adolf,Kostikov, Rafael R.

, p. 133 - 137 (2007/10/03)

Iminiodifluoromethanides generated by the reaction of difluorocarbene with benzaldehyde and benzophenone imines undergo regioselective 1,3-dipolar cycloaddition to aldehydes to give oxazolidine derivatives.

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