Cas 14928-77-9,Acetamide, 2,2,2-trifluoro-N-phenyl-N-(phenylmethyl)-

14928-77-9

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Basic information

Product Name: Acetamide, 2,2,2-trifluoro-N-phenyl-N-(phenylmethyl)-
Synonyms:
CAS NO:14928-77-9
Molecular Formula: C15H12F3NO
Molecular Weight: 279.262
EINECS: N/A
Product Categories: N/A
Mol File: 14928-77-9.mol

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: Acetamide, 2,2,2-trifluoro-N-phenyl-N-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-phenyl-N-(phenylmethyl)-(14928-77-9)
EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-phenyl-N-(phenylmethyl)-(14928-77-9)

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: 14928-77-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 14928-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14928-77:
(7*1)+(6*4)+(5*9)+(4*2)+(3*8)+(2*7)+(1*7)=129
129 % 10 = 9
So 14928-77-9 is a valid CAS Registry Number.

14928-77-9Upstream product

14928-77-9Downstream Products

14928-77-9Relevant academic research and scientific papers

Efficient DBU accelerated synthesis of 18F-labelled trifluoroacetamides

Gómez, Antonio Bermejo,Cortés González, Miguel A.,Lübcke, Marvin,Johansson, Magnus J.,Halldin, Christer,Szabó, Kálmán J.,Schou, Magnus

supporting information, p. 13963 - 13966 (2016/12/09)

Nucleophilic 18F-fluorination of bromodifluoromethyl derivatives was performed using [18F]Bu4NF in the presence of DBU (1,8-diazabicyclo[5.4.0]undec-7-ene). This novel procedure provided a diverse set of [18F]trifluoroacetamides in good to excellent radiochemical conversions. A mechanism where DBU acts as organomediator in this transformation is proposed.

Reductive amination without an external hydrogen source

Chusov, Denis,List, Benjamin

supporting information, p. 5199 - 5201 (2014/05/20)

A method of reductive amination without an external hydrogen source is reported. Carbon monoxide is used as the reductant. The reaction proceeds efficiently for a variety of carbonyl compounds and amines at low catalyst loadings and is mechanistically interesting as it does not seem to involve molecular hydrogen. Look, no H2! Reductive amination without an external hydrogen source has been developed using carbon monoxide as the reductant and rhodium acetate (0.2-1mol %) as catalyst. The method tolerates a variety of functional groups and provides target amines in good to excellent yields.

One-Step Hydroamidation of a Schiff Base with Trichlorosilane

Okamoto, Hidenori,Kato, Shozo

, p. 2128 - 2130 (2007/10/02)

We have found that the treatment of a Schiff base (2) with trichlorosilane and chloroacetyl chloride results in a highly active chloroacetamide herbicide (1) in an excellent yield .This one-step hydroamidation reaction of a Schiff base is a useful synthet

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