Cas 135679-83-3,N-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide

135679-83-3

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Basic information

Product Name: N-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide
Synonyms: N-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide
CAS NO:135679-83-3
Molecular Formula:
Molecular Weight: 298.308
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-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide(135679-83-3)
EPA Substance Registry System: N-[4-(Benzyl-methyl-amino)-but-2-ynyl]-2,2,2-trifluoro-N-methyl-acetamide(135679-83-3)

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: 135679-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135679-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135679-83:
(8*1)+(7*3)+(6*5)+(5*6)+(4*7)+(3*9)+(2*8)+(1*3)=163
163 % 10 = 3
So 135679-83-3 is a valid CAS Registry Number.

135679-83-3Upstream product

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135679-83-3Relevant academic research and scientific papers

Highly selective TFAA-cleavage of tertiary 2,4-dimethoxybenzylamines and its use in the synthesis of secondary amines

Nussbaumer,Baumann,Dechat,Harasek

, p. 4591 - 4602 (2007/10/02)

TFAA-treatment of allylic, propargylic, homopropargylic and some benzylic tert. 2, 4-dimethoxybenzylamines leads to highly selective cleavage of their dimethoxybenzylic C-N bonds. The resultant trifluoroacetamides can then readily be converted to the corresponding secondary amines.

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