Cas 1275592-82-9,tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate

1275592-82-9

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Basic information

Product Name: tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate
Synonyms: tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate
CAS NO:1275592-82-9
Molecular Formula:
Molecular Weight: 633.903
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: tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate(1275592-82-9)
EPA Substance Registry System: tert-butyl 2-(2-benzyloxyethyl)-3-(2-tert-butyldiphenylsiloxyethyl)-1H-indole-1-carboxylate(1275592-82-9)

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: 1275592-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1275592-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,5,5,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1275592-82:
(9*1)+(8*2)+(7*7)+(6*5)+(5*5)+(4*9)+(3*2)+(2*8)+(1*2)=189
189 % 10 = 9
So 1275592-82-9 is a valid CAS Registry Number.

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1275592-82-9Relevant academic research and scientific papers

Total syntheses of (-)- and (+)-goniomitine

Mizutani, Masaya,Inagaki, Fuyuhiko,Nakanishi, Takeo,Yanagihara, Chihiro,Tamai, Ikumi,Mukai, Chisato

, p. 1796 - 1799 (2011/06/19)

The Stille coupling reaction of 3-(benzyloxymethyl)-1-(tert- butyldiphenylsiloxy)ethyl-1-(tributylstannyl)allene with N-(tert-butoxycarbonyl) -2-iodoaniline directly produced the corresponding 2-vinylindole derivative, which was independently transformed

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