Cas 710-01-0,1-(3-Amino-phenyl)-2-trifluormethyl-aethylen

710-01-0

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Basic information

Product Name: 1-(3-Amino-phenyl)-2-trifluormethyl-aethylen
Synonyms: 1-(3-Amino-phenyl)-2-trifluormethyl-aethylen
CAS NO:710-01-0
Molecular Formula:
Molecular Weight: 187.164
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: 1-(3-Amino-phenyl)-2-trifluormethyl-aethylen(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-Amino-phenyl)-2-trifluormethyl-aethylen(710-01-0)
EPA Substance Registry System: 1-(3-Amino-phenyl)-2-trifluormethyl-aethylen(710-01-0)

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: 710-01-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 710-01-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 710-01:
(5*7)+(4*1)+(3*0)+(2*0)+(1*1)=40
40 % 10 = 0
So 710-01-0 is a valid CAS Registry Number.

710-01-0Upstream product

718-14-9 1-nitro-3-(3,3,3-trifluoroprop-1-en-1-yl)benzene

710-01-0Downstream Products

710-01-0Relevant academic research and scientific papers

Deoxofluorination of (Hetero)aromatic Acids

Alekseenko, Anatoliy N.,Bugera, Maksym Ya.,Gerus, Igor I.,Kiriakov, Oleksandr,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Pustovit, Yurii,Razhyk, Bohdan,Semenov, Sergey,Starova, Viktoriia S.,Tananaiko, Oksana Yu.,Tarasenko, Karen,Tolmachev, Andrei A.,Trofymchuk, Serhii,Zaporozhets, Olga A.

, p. 3110 - 3124 (2020)

Diverse trifluoromethyl-substituted compounds were synthesized by deoxofluorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride. The obtained products were used as starting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building blocks for medicinal chemistry and agrochemistry.

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