Cas 211615-75-7,4-[5-Bromo-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine

211615-75-7

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Basic information

Product Name: 4-[5-Bromo-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine
Synonyms:
CAS NO:211615-75-7
Molecular Formula:
Molecular Weight: 460.446
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: 4-[5-Bromo-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 4-[5-Bromo-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine(211615-75-7)
EPA Substance Registry System: 4-[5-Bromo-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine(211615-75-7)

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: 211615-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 211615-75-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,6,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 211615-75:
(8*2)+(7*1)+(6*1)+(5*6)+(4*1)+(3*5)+(2*7)+(1*5)=97
97 % 10 = 7
So 211615-75-7 is a valid CAS Registry Number.

211615-75-7Upstream product

1120-87-2 4-bromopyridin

211615-75-7Downstream Products

1027900-70-4 4-[5-(4-Fluoro-phenyl)-2-(4-methoxy-phenyl)-3-(2-trimethylsilanyl-ethoxymethyl)-3H-imidazol-4-yl]-pyridine

211615-75-7Relevant academic research and scientific papers

Vicinal bromostannanes as novel building blocks for the preparation of di- and trisubstituted imidazoles

Revesz, Laszlo,Bonne, Frederique,Makavou, Paschalia

, p. 5171 - 5174 (1998)

Three novel imidazole-based vicinal bromostannanes 5a-c have been developed for the regioselective preparation of 2,4,5-tri- and 4,5- disubstituted imidazoles. The novel building blocks are particularly attractive for Stille and Suzuki couplings that invo

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