Cas 1204591-53-6,3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione

1204591-53-6

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Product Name: 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione
Synonyms: 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione
CAS NO:1204591-53-6
Molecular Formula:
Molecular Weight: 646.632
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: 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione(1204591-53-6)
EPA Substance Registry System: 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-(((1S)-((2S,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)amino)cyclobut-3-ene-1,2-dione(1204591-53-6)

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Hazard Codes: N/A
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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1204591-53-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1204591-53-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,5,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1204591-53:
(9*1)+(8*2)+(7*0)+(6*4)+(5*5)+(4*9)+(3*1)+(2*5)+(1*3)=126
126 % 10 = 6
So 1204591-53-6 is a valid CAS Registry Number.

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1204591-53-6Relevant academic research and scientific papers

Highly enantioselective phosphination and hydrophosphonylation of azomethine imines: Using chiral squaramide as a hydrogen bonding organocatalyst

Kong, Ling-Pei,Li, Nai-Kai,Zhang, Shao-Yun,Chen, Xiang,Zhao, Min,Zhang, Ya-Fei,Wang, Xing-Wang

, p. 8656 - 8670 (2014/12/10)

Enantioselective phosphination and hydrophosphonylation reactions between azomethine imines and diarylphosphine oxides or dialkyl phosphites were respectively developed by the use of a chiral squaramide as the hydrogen bonding organocatalyst, which afforded two types of phosphorus containing product in high yields with good to excellent enantioselectivities.

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