Cas 1032192-18-9,2,2,2-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide

1032192-18-9

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Basic information

Product Name: 2,2,2-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide
Synonyms: 2,2,2-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide
CAS NO:1032192-18-9
Molecular Formula:
Molecular Weight: 373.372
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-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide(1032192-18-9)
EPA Substance Registry System: 2,2,2-trifluoro-N-(4-methoxyphenyl)-N-((2R)-1-(tetrahydro-2H-pyran-2-yloxy)but-3-en-2-yl)acetamide(1032192-18-9)

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: 1032192-18-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1032192-18-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,1,9 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1032192-18:
(9*1)+(8*0)+(7*3)+(6*2)+(5*1)+(4*9)+(3*2)+(2*1)+(1*8)=99
99 % 10 = 9
So 1032192-18-9 is a valid CAS Registry Number.

1032192-18-9Upstream product

1032191-89-1 ((Z)-4-(tetrahydro-2H-pyran-2-yloxy)but-2-enyl)-2,2,2-trifluoro-N-(4-methoxyphenyl)acetimidate

1032192-18-9Downstream Products

1032192-20-3 (-)-(2R)-2-[(4-methoxyphenyl)amino]but-3-en-1-ol

1032192-18-9Relevant academic research and scientific papers

Synthesis of nearly enantiopure allylic amines by aza-Claisen rearrangement of Z-configured allylic trifluoroacetimidates catalyzed by highly active ferrocenylbispalladacycles

Jautze, Sascha,Seiler, Paul,Peters, Rene

experimental part, p. 1430 - 1444 (2009/04/06)

The development of the first highly active enantioselective catalyst for the aza-Claisen rearrangement of Z-configured allylic trifluoroacetimidates generating valuable almost enantiopure protected allylic amines is described. Usually Z-configured allylic

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