Cas 156426-86-7,(2S,3S)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-3-hydroxy-2-methyl-4-phenyl-butane-1,4-dione

156426-86-7

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Basic information

Product Name: (2S,3S)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-hydroxy-2-methyl-4-phenyl-butane-1,4-dione
Synonyms:
CAS NO:156426-86-7
Molecular Formula:
Molecular Weight: 405.515
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)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-hydroxy-2-methyl-4-phenyl-butane-1,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-hydroxy-2-methyl-4-phenyl-butane-1,4-dione(156426-86-7)
EPA Substance Registry System: (2S,3S)-1-((1S,5R,7R)-10,10-Dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-3-hydroxy-2-methyl-4-phenyl-butane-1,4-dione(156426-86-7)

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: 156426-86-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 156426-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,4,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 156426-86:
(8*1)+(7*5)+(6*6)+(5*4)+(4*2)+(3*6)+(2*8)+(1*6)=147
147 % 10 = 7
So 156426-86-7 is a valid CAS Registry Number.

156426-86-7Upstream product

1074-12-0 phenylglyoxal hydrate

156426-86-7Downstream Products

185628-39-1 Acetic acid (2S,3R)-2,4-diacetoxy-3-methyl-1-phenyl-butyl ester

156426-86-7Relevant academic research and scientific papers

Diastereo-face selectivity in the aldol reaction of boryl enolate derived from Oppolzer's sultam

Iseki, Katsuhiko,Oishi, Satoshi,Kobayashi, Yoshiro

, p. 2003 - 2008 (1996)

In the Oppolzer aldol reaction, aldehyde reacts exclusively on the Si face (C(α)-Si attack) of the double bond of the boryl enolate 2 derived from (1S,2R)-N-propionylbornane-10,2-sultam (1), providing only 3a stereoselectively. Hexafluoroacetone (4) cause

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