Cas 1025823-13-5,(2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid

1025823-13-5

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Basic information

Product Name: (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid
Synonyms: (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid
CAS NO:1025823-13-5
Molecular Formula:
Molecular Weight: 443.567
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: (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid(1025823-13-5)
EPA Substance Registry System: (2S,3S,6S)-1-Dimethylamino-6-((S)-hydroxy-phenyl-methyl)-2-((R)-1-phenyl-ethylcarbamoyl)-1,2,3,6-tetrahydro-pyridine-3-sulfinic acid(1025823-13-5)

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: 1025823-13-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1025823-13-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,8,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1025823-13:
(9*1)+(8*0)+(7*2)+(6*5)+(5*8)+(4*2)+(3*3)+(2*1)+(1*3)=115
115 % 10 = 5
So 1025823-13-5 is a valid CAS Registry Number.

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1025823-13-5Relevant academic research and scientific papers

Three-component sequential Aza[4+2] cycloaddition/allylboration/retro- sulfinyl-ene reaction: A new stereocontrolled entry to palustrine alkaloids and other 2,6-disubstituted piperidines

Toure, Barry B.,Hall, Dennis G.

, p. 2001 - 2004 (2007/10/03)

Step-economy and stereocontrol are highlighted in a novel three-component sequential reaction to access substituted piperidines (see scheme). Through combining boronate-substituted hydrazonobutadienes, chiral sulfinimide dienophiles, and aldehydes in a hi

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