Cas 1607826-75-4,ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate

1607826-75-4

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Basic information

Product Name: ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate
Synonyms: ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate
CAS NO:1607826-75-4
Molecular Formula:
Molecular Weight: 599.591
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: ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate(1607826-75-4)
EPA Substance Registry System: ethyl 5-bromo-1-methyl-3-[2-(tritylsulfanyl)ethyl]amino-1H-indole-2-carboxylate(1607826-75-4)

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: 1607826-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1607826-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,7,8,2 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1607826-75:
(9*1)+(8*6)+(7*0)+(6*7)+(5*8)+(4*2)+(3*6)+(2*7)+(1*5)=184
184 % 10 = 4
So 1607826-75-4 is a valid CAS Registry Number.

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1607826-75-4Relevant academic research and scientific papers

Copper-catalyzed intermolecular C-H amination of (Hetero)arenes via transient unsymmetrical λ3-iodanes

Sokolovs, Igors,Lubriks, Dmitrijs,Suna, Edgars

, p. 6920 - 6928 (2014/06/09)

A one-pot two-step method for intermolecular C-H amination of electron-rich heteroarenes and arenes has been developed. The approach is based on a room-temperature copper-catalyzed regioselective reaction of the in situ formed unsymmetrical (hetero)aryl-λ3-iodanes with a wide range of primary and secondary aliphatic amines and anilines.

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