Cas 1449581-69-4,N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride

1449581-69-4

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Basic information

Product Name: N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride
Synonyms: N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride
CAS NO:1449581-69-4
Molecular Formula:
Molecular Weight: 519.914
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: N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride(1449581-69-4)
EPA Substance Registry System: N,N-dibenzyl-1-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)methanamine hydrochloride(1449581-69-4)

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: 1449581-69-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449581-69-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,5,8 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1449581-69:
(9*1)+(8*4)+(7*4)+(6*9)+(5*5)+(4*8)+(3*1)+(2*6)+(1*9)=204
204 % 10 = 4
So 1449581-69-4 is a valid CAS Registry Number.

1449581-69-4Upstream product

1449581-56-9 C₂₅H₂₁F₆NO₃

1449581-69-4Downstream Products

1449581-69-4Relevant academic research and scientific papers

Amide activation by TMSCl: Reduction of amides to amines by LiAlH 4 under mild conditions

Ravinder,Rajeswar Reddy,Panasa Reddy,Bandichhor, Rakeshwar

, p. 4908 - 4913 (2013)

An expeditious and practical method for the reduction of amides to amines is reported. The method consists of activation of amides with TMSCl followed by reduction with LiAlH4. Various amides/lactams including hindered amides and secondary amides gave the corresponding amines in good to excellent yields. This novel protocol has a wide substrate scope and shows good functional group tolerance with high stereoretention.

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