Cas 1027260-18-9,Carbonic acid ethyl ester (E)-3-{(1R,2R)-2-[((R)-1-phenyl-ethyl)-(3-trimethylsilanyl-prop-2-ynyl)-amino]-cyclohexyl}-allyl ester

1027260-18-9

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Basic information

Product Name: Carbonic acid ethyl ester (E)-3-{(1R,2R)-2-[((R)-1-phenyl-ethyl)-(3-trimethylsilanyl-prop-2-ynyl)-amino]-cyclohexyl}-allyl ester
Synonyms:
CAS NO:1027260-18-9
Molecular Formula:
Molecular Weight: 441.686
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: Carbonic acid ethyl ester (E)-3-{(1R,2R)-2-[((R)-1-phenyl-ethyl)-(3-trimethylsilanyl-prop-2-ynyl)-amino]-cyclohexyl}-allyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbonic acid ethyl ester (E)-3-{(1R,2R)-2-[((R)-1-phenyl-ethyl)-(3-trimethylsilanyl-prop-2-ynyl)-amino]-cyclohexyl}-allyl ester(1027260-18-9)
EPA Substance Registry System: Carbonic acid ethyl ester (E)-3-{(1R,2R)-2-[((R)-1-phenyl-ethyl)-(3-trimethylsilanyl-prop-2-ynyl)-amino]-cyclohexyl}-allyl ester(1027260-18-9)

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: 1027260-18-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027260-18-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,2,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1027260-18:
(9*1)+(8*0)+(7*2)+(6*7)+(5*2)+(4*6)+(3*0)+(2*1)+(1*8)=109
109 % 10 = 9
So 1027260-18-9 is a valid CAS Registry Number.

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1027260-18-9Relevant academic research and scientific papers

Stereoselective synthesis of optically active substituted piperidines and pyrrolidines from amino acid derivatives by titanium(II)mediated intramolecular cyclization reaction

Takayama, Yuuki,Okamoto, Sentaro,Sato, Fumie

, p. 8351 - 8354 (2007/10/03)

A versatile and high-yielding synthesis of optically active substituted piperidines and pyrrolidines from amino acid derivatives employing titanium(II)mediated intramolecular cyclization of bis-unsaturated carbonates was developed.

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