Cas 1190130-56-3,4-(4-methoxybenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine

1190130-56-3

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Basic information

Product Name: 4-(4-methoxybenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine
Synonyms:
CAS NO:1190130-56-3
Molecular Formula:
Molecular Weight: 311.307
EINECS: N/A
Product Categories: N/A
Mol File: 1190130-56-3.mol
Article Data: 1

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-(4-methoxybenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-methoxybenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(1190130-56-3)
EPA Substance Registry System: 4-(4-methoxybenzyl)-4-trifluoromethyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(1190130-56-3)

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: 1190130-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190130-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,1,3 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1190130-56:
(9*1)+(8*1)+(7*9)+(6*0)+(5*1)+(4*3)+(3*0)+(2*5)+(1*6)=113
113 % 10 = 3
So 1190130-56-3 is a valid CAS Registry Number.

1190130-56-3Upstream product

56-92-8 histamine dichloride

1190130-56-3Downstream Products

1190130-56-3Relevant articles and documents

α-Trifluoromethyl-β-aryl enamines in the synthesis of trifluoromethylated heterocycles by the Fischer and the Pictet-Spengler reactions

Muzalevskiy, Vasiliy M.,Nenajdenko, Valentine G.,Shastin, Aleksey V.,Balenkova, Elizabeth S.,Haufe, Günter

experimental part, p. 7553 - 7561 (2009/12/06)

α-Trifluoromethyl-β-aryl enamines were successfully used as synthetic equivalents of benzyltrifluoromethyl ketones in both the Fischer indole synthesis and the Pictet-Spengler reaction. Accordingly, 2-trifluoromethyl indoles and a variety of trifluorometh

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