Cas 869708-45-2,Pyridine, 1-(2,2-dimethyl-1-oxopropyl)-1,4-dihydro-3-[(2S)-1-methyl-2-pyrrolidinyl] -4-(phenylmethyl)-, (4S)-

869708-45-2

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Basic information

Product Name: Pyridine, 1-(2,2-dimethyl-1-oxopropyl)-1,4-dihydro-3-[(2S)-1-methyl-2-pyrrolidinyl] -4-(phenylmethyl)-, (4S)-
Synonyms:
CAS NO:869708-45-2
Molecular Formula: C22H30N2O
Molecular Weight: 338.493
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: Pyridine, 1-(2,2-dimethyl-1-oxopropyl)-1,4-dihydro-3-[(2S)-1-methyl-2-pyrrolidinyl] -4-(phenylmethyl)-, (4S)-(CAS DataBase Reference)
NIST Chemistry Reference: Pyridine, 1-(2,2-dimethyl-1-oxopropyl)-1,4-dihydro-3-[(2S)-1-methyl-2-pyrrolidinyl] -4-(phenylmethyl)-, (4S)-(869708-45-2)
EPA Substance Registry System: Pyridine, 1-(2,2-dimethyl-1-oxopropyl)-1,4-dihydro-3-[(2S)-1-methyl-2-pyrrolidinyl] -4-(phenylmethyl)-, (4S)-(869708-45-2)

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: 869708-45-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869708-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,7,0 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 869708-45:
(8*8)+(7*6)+(6*9)+(5*7)+(4*0)+(3*8)+(2*4)+(1*5)=232
232 % 10 = 2
So 869708-45-2 is a valid CAS Registry Number.

869708-45-2Upstream product

869708-45-2Downstream Products

869708-45-2Relevant academic research and scientific papers

Synthesis of C-4 substituted nicotine derivatives via an N-acylpyridinium salt of (S)-nicotine

Comins, Daniel L.,King, Laura S.,Smith, Emilie D.,Fevrier, Florence C.

, p. 5059 - 5062 (2005)

(Chemical Equation Presented) A variety of novel nicotine derivatives were prepared from (S)-nicotine via a two-step sequence. Addition of a cuprate reagent to an N-acylpyridinium salt of nicotine, followed by aromatization with elemental sulfur, afforded

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