Cas 1447640-64-3,ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate

1447640-64-3

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Basic information

Product Name: ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate
Synonyms: ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate
CAS NO:1447640-64-3
Molecular Formula:
Molecular Weight: 334.366
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: ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate(1447640-64-3)
EPA Substance Registry System: ethyl 2-(4-amino-2-fluoro-6-methylphenyl)-2-((3-fluoro-5-methylphenyl)amino)acetate(1447640-64-3)

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: 1447640-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1447640-64-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,7,6,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1447640-64:
(9*1)+(8*4)+(7*4)+(6*7)+(5*6)+(4*4)+(3*0)+(2*6)+(1*4)=173
173 % 10 = 3
So 1447640-64-3 is a valid CAS Registry Number.

1447640-64-3Upstream product

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1447640-64-3Relevant academic research and scientific papers

A catalyst-free N-H insertion/Mannich-type reaction cascade of α-nitrodiazoesters

Yang, Ting,Zhuang, Hao,Lin, Xichen,Xiang, Jia-Ning,Elliott, John D.,Liu, Lianghui,Ren, Feng

supporting information, p. 4159 - 4163 (2013/07/26)

A catalyst-free N-H insertion/Mannich-type reaction cascade of α-nitrodiazoesters with anilines has been developed to afford a variety of α-amino-α-aryl esters in 60-83% yields and under mild reaction conditions (23 or 40 C).

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