Cas 839673-20-0,Carbamic acid, [(1S,2S)-1-(1H-indol-3-ylmethyl)-2-[[(4-methylphenyl)sulfonyl]oxy]propyl]- , 1,1-dimethylethyl ester

839673-20-0

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Basic information

Product Name: Carbamic acid, [(1S,2S)-1-(1H-indol-3-ylmethyl)-2-[[(4-methylphenyl)sulfonyl]oxy]propyl]- , 1,1-dimethylethyl ester
Synonyms:
CAS NO:839673-20-0
Molecular Formula: C24H30N2O5S
Molecular Weight: 458.579
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: Carbamic acid, [(1S,2S)-1-(1H-indol-3-ylmethyl)-2-[[(4-methylphenyl)sulfonyl]oxy]propyl]- , 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S,2S)-1-(1H-indol-3-ylmethyl)-2-[[(4-methylphenyl)sulfonyl]oxy]propyl]- , 1,1-dimethylethyl ester(839673-20-0)
EPA Substance Registry System: Carbamic acid, [(1S,2S)-1-(1H-indol-3-ylmethyl)-2-[[(4-methylphenyl)sulfonyl]oxy]propyl]- , 1,1-dimethylethyl ester(839673-20-0)

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: 839673-20-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 839673-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,9,6,7 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 839673-20:
(8*8)+(7*3)+(6*9)+(5*6)+(4*7)+(3*3)+(2*2)+(1*0)=210
210 % 10 = 0
So 839673-20-0 is a valid CAS Registry Number.

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839673-20-0Relevant academic research and scientific papers

The diastereoselective synthesis of quaternary substituted thioindolines from sulfur ylide intermediates

Nyong, Abijah M.,Rainier, Jon D.

, p. 746 - 748 (2005)

(Chemical Equation Presented) The Rh(II)-catalyzed coupling of chiral 2-thiopyranylindoles with vinyl diazoacetates results in the generation of indolines having quaternary substitution at C(3) in high diastereoselectivity.

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