Cas 1609286-29-4,(S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride

1609286-29-4

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Basic information

Product Name: (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride
Synonyms: (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride
CAS NO:1609286-29-4
Molecular Formula:
Molecular Weight: 331.285
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: (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride(1609286-29-4)
EPA Substance Registry System: (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane chloride(1609286-29-4)

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: 1609286-29-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609286-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,2,8 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1609286-29:
(9*1)+(8*6)+(7*0)+(6*9)+(5*2)+(4*8)+(3*6)+(2*2)+(1*9)=184
184 % 10 = 4
So 1609286-29-4 is a valid CAS Registry Number.

1609286-29-4Upstream product

1609286-29-4Downstream Products

1609286-36-3 (S)-2-((R)-1-(benzyloxy)ethyl)-1-(chloromethyl)-1,4-diazabicyclo[2.2.2]octane trifluoromethanesulfonate

1609286-29-4Relevant academic research and scientific papers

CHIRAL FLUORINATING REAGENTS

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, (2014/05/24)

This invention relates to fluorinating agents and, more particularly, to chiral non-racemic fluorinating agents useful for enantioselective fluorination, as well as to their synthesis and use and other subject matter. The fluorinating agents are based on a substituted 1,4-diazabicyclo[2.2.2]octane (DABCO) skeleton and provide electrophillic fluorine enantioselectively.

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