Cas 1504592-08-8,tert-butyl 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate

1504592-08-8

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Basic information

Product Name: tert-butyl 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate
Synonyms: tert-butyl 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate
CAS NO:1504592-08-8
Molecular Formula:
Molecular Weight: 465.503
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 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate(1504592-08-8)
EPA Substance Registry System: tert-butyl 3-((2-formyl-3,6-bis(methoxymethoxy)phenyl)ethynyl)-1H-indole-1-carboxylate(1504592-08-8)

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: 1504592-08-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1504592-08-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,0,4,5,9 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1504592-08:
(9*1)+(8*5)+(7*0)+(6*4)+(5*5)+(4*9)+(3*2)+(2*0)+(1*8)=148
148 % 10 = 8
So 1504592-08-8 is a valid CAS Registry Number.

1504592-08-8Upstream product

129896-49-7 tert-butyl 3-ethynyl-1H-indole-1-carboxylate

1504592-08-8Downstream Products

1570188-51-0 C₃₀H₃₆N₂O₆

1504592-08-8Relevant academic research and scientific papers

Total synthesis of the marine alkaloid mansouramycin D

Prakash,Nagarajan, Rajagopal

, p. 244 - 246 (2014)

Mansouramycin D, a cytotoxic alkaloid was isolated from a marine Streptomyces sp. in 2009. The first, simple, and concise route to the total synthesis of Mansouramycin D is reported. The core structure of the isoquinoline ring has been constructed from iminoannulation of 2-alkynylbenzaldehyde followed by oxidation/deprotection and oxidative amination via a three-step sequence from easily accessible starting materials.

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