Cas 181574-76-5,N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide

181574-76-5

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Basic information

Product Name: N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide
Synonyms: N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide
CAS NO:181574-76-5
Molecular Formula:
Molecular Weight: 412.393
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: N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide(181574-76-5)
EPA Substance Registry System: N-(4-Benzyloxy-1-nitro-naphthalen-2-yl)-N-(3,3-difluoro-allyl)-acetamide(181574-76-5)

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: 181574-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181574-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,5,7 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 181574-76:
(8*1)+(7*8)+(6*1)+(5*5)+(4*7)+(3*4)+(2*7)+(1*6)=155
155 % 10 = 5
So 181574-76-5 is a valid CAS Registry Number.

181574-76-5Upstream product

181574-75-4 3-[N-(3,3-Difluoro-2-propen-1-yl)acetamido]-1-benzyloxynaphthalene

181574-76-5Downstream Products

181574-76-5Relevant academic research and scientific papers

Synthesis, X-ray structure, and properties of fluorocyclopropane analogs of the duocarmycins incorporating the 9,9-difluoro-1,2,9,9a-tetrahydrocyclopropa[c]benzo[e]indol-4-one (F2CBI) alkylation subunit

Boger, Dale L.,Jenkins, Tracy J.

, p. 8860 - 8870 (1996)

The synthesis of 9,9-difluoro-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (F2CBI), a difluorocyclopropane analog of the CC-1065 and duocarmycin alkylation subunits which represents the first such agent containing substitution of the reac

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