Cas 1046786-41-7,2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile

1046786-41-7

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Basic information

Product Name: 2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile
Synonyms: 2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile
CAS NO:1046786-41-7
Molecular Formula:
Molecular Weight: 332.248
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: 2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile(1046786-41-7)
EPA Substance Registry System: 2-[2,2-bis(trifluoromethyl)-1-phenylbutylidene]malononitrile(1046786-41-7)

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: 1046786-41-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1046786-41-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,7,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1046786-41:
(9*1)+(8*0)+(7*4)+(6*6)+(5*7)+(4*8)+(3*6)+(2*4)+(1*1)=167
167 % 10 = 7
So 1046786-41-7 is a valid CAS Registry Number.

1046786-41-7Upstream product

68761-08-0 (1-phenyl-butylidene)-malononitrile

1046786-41-7Downstream Products

1046786-41-7Relevant academic research and scientific papers

Fluorinated Johnson reagent for transfer-trifluoromethylation to carbon nucleophiles

Noritake, Shun,Shibata, Norio,Nakamura, Shuichi,Toru, Takeshi,Shiro, Motoo

supporting information; experimental part, p. 3465 - 3468 (2009/04/08)

A novel reagent, [(oxido)phenyl(trifluoromethyl)-λ4- sulfanylidene] dimethylammonium tetrafluoroborate has been developed for the electrophilic trifluoromethylation of carbon nucleophiles. The reagent was designed as a trifluorinated version of

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