Cas 1620051-28-6,3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide

1620051-28-6

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Basic information

Product Name: 3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide
Synonyms: 3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide
CAS NO:1620051-28-6
Molecular Formula:
Molecular Weight: 345.374
EINECS: N/A
Product Categories: N/A
Mol File: 1620051-28-6.mol
Article Data: 1

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: 3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide(1620051-28-6)
EPA Substance Registry System: 3-(3-fluoro-4-nitrophenyl)-N-(2-(pyridin-2-yl)propan-2-yl)butanamide(1620051-28-6)

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: 1620051-28-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620051-28-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,0,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1620051-28:
(9*1)+(8*6)+(7*2)+(6*0)+(5*0)+(4*5)+(3*1)+(2*2)+(1*8)=106
106 % 10 = 6
So 1620051-28-6 is a valid CAS Registry Number.

1620051-28-6Upstream product

1620051-28-6Downstream Products

1620051-28-6Relevant articles and documents

Pd(ii)-Catalyzed arylation of unactivated methylene C(sp3)-H bonds with aryl halides using a removable auxiliary

Zhang, Qi,Yin, Xue-Song,Zhao, Sheng,Fang, Sheng-Long,Shi, Bing-Feng

supporting information, p. 8353 - 8355 (2014/07/22)

A Pd(ii)-catalyzed arylation of methylene C(sp3)-H bonds in aliphatic amides directed by our newly developed PIP directing group with aryl iodides/bromides has been achieved. Arylation occurs efficiently with a broad range of aryl halides and amides. This journal is the Partner Organisations 2014.

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