Cas 1209485-59-5,(1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate

1209485-59-5

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Basic information

Product Name: (1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate
Synonyms:
CAS NO:1209485-59-5
Molecular Formula:
Molecular Weight: 596.478
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: (1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate(1209485-59-5)
EPA Substance Registry System: (1R,2R)-2-(dipropylamino)cyclohexanaminium 1,1,2,2-tetrafluoro-2-(1,1,2,2,3,3,4,4-octafluorobutoxy)ethanesulfonate(1209485-59-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1209485-59-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1209485-59-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,9,4,8 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1209485-59:
(9*1)+(8*2)+(7*0)+(6*9)+(5*4)+(4*8)+(3*5)+(2*5)+(1*9)=165
165 % 10 = 5
So 1209485-59-5 is a valid CAS Registry Number.

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1209485-59-5Relevant academic research and scientific papers

Enantioselective aldol reaction of cyclic ketones with aryl aldehydes catalyzed by a cyclohexanediamine derived salt in the presence of water

Lin, Jin-Hong,Zhang, Cheng-Pan,Xiao, Ji-Chang

, p. 1750 - 1753 (2009)

Water was found to be a suitable reaction medium for the direct asymmetric aldol reaction of various cyclic ketones with aryl aldehydes catalyzed by a primary-tertiary diamine-Bronsted acid. The Royal Society of Chemistry 2009.

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