Cas 339193-69-0,methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[<i>cd</i>]indol-4-yl]-carbamic acid <i>tert</i>-butyl ester

339193-69-0

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Basic information

Product Name: methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid tert-butyl ester
Synonyms: methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid tert-butyl ester
CAS NO:339193-69-0
Molecular Formula:
Molecular Weight: 452.574
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: methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid tert-butyl ester(339193-69-0)
EPA Substance Registry System: methyl-[5-methylene-1-(toluene-4-sulfonyl)-1,3,4,5-tetrahydro-benzo[cd]indol-4-yl]-carbamic acid tert-butyl ester(339193-69-0)

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: 339193-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 339193-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,9,1,9 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 339193-69:
(8*3)+(7*3)+(6*9)+(5*1)+(4*9)+(3*3)+(2*6)+(1*9)=170
170 % 10 = 0
So 339193-69-0 is a valid CAS Registry Number.

339193-69-0Upstream product

339193-67-8 {1-[4-bromo-1-(toluene-4-sulfonyl)-1H-indol-3-ylmethyl]-3-trimethylsilanyl-prop-2-ynyl}-methyl-carbamic acid tert-butyl ester

339193-69-0Downstream Products

339193-69-0Relevant academic research and scientific papers

Novel entry to the Ergot alkaloids via ring closing metathesis

Lee, Katherine L.,Goh, Jane Betty,Martin, Stephen F.

, p. 1635 - 1638 (2001)

A novel entry the Ergot alkaloids has been developed. It features a Heck reaction followed by hydride capture to generate the key tricyclic intermediate 12 and a ring closing metathesis reaction to give the tetracyclic ergoline ring system 3.

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