Cas 194656-48-9,(R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone

194656-48-9

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Basic information

Product Name: (R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone
Synonyms: (R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone
CAS NO:194656-48-9
Molecular Formula:
Molecular Weight: 349.546
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: (R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone(CAS DataBase Reference)
NIST Chemistry Reference: (R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone(194656-48-9)
EPA Substance Registry System: (R)-4-Isopropyl-4-((S)-2-methoxymethyl-pyrrolidine-1-carbonyl)-3-trimethylsilanyl-cyclohexa-2,5-dienone(194656-48-9)

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: 194656-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194656-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,6,5 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 194656-48:
(8*1)+(7*9)+(6*4)+(5*6)+(4*5)+(3*6)+(2*4)+(1*8)=179
179 % 10 = 9
So 194656-48-9 is a valid CAS Registry Number.

194656-48-9Upstream product

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194656-48-9Relevant academic research and scientific papers

Asymmetric synthesis of 4,4-disubstituted-2-cyclohexen-1-ones from a chiral 2-(trimethylsilyl)benzamide

Schultz, Arthur G.,Pettus, Liping

, p. 5433 - 5436 (1997)

Birch reduction-alkylation of the chiral 2-(trimethylsilyl)benzamide 4 provides 1,4-cyclohexadienes 5b-5e with diastereomer ratios of >100:1. The conversions of 5b-5e to the 4,4-disubstituted-2-cyclohexen-1-ones 8b-8e are described.

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