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N,N-diethyl-2-{4-[(E)-2-phenylethenyl]phenoxy}ethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73675-52-2

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73675-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73675-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73675-52:
(7*7)+(6*3)+(5*6)+(4*7)+(3*5)+(2*5)+(1*2)=152
152 % 10 = 2
So 73675-52-2 is a valid CAS Registry Number.

73675-52-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-diethyl-2-[4-[(E)-2-phenylethenyl]phenoxy]ethanamine

1.2 Other means of identification

Product number -
Other names 4-(2-Diaethylamino-aethoxy)-trans-stilben

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73675-52-2 SDS

73675-52-2Relevant academic research and scientific papers

Synthesis of trans-N,N,N-triethyl-2-ethanammonium iodide

Al-Hassan, Mohammed I.

, p. 395 - 397 (1990)

The antispasmodic olefin trans-N,N,N-triethyl-2-ethanammonium iodide has been made by hydroalumination of a trimethylsilylalkyne followed by palladium-catalyzed cross-coupling of the vinylalane with the appropriate aryl bromide.

Synthesis of N,N,N-Triethyl-2-ethanammonium iodide.

Al-Hassan, Mohammed I.

, p. 1677 - 1680 (2007/10/02)

The synthesis of N,N,N-triethyl-2-ethanammonium iodide, antispasmodic disubstituted olefin, was achieved via palladium-catalyzed cross-coupling of phenylacetylide with aryl bromide followed by hydroalumination.

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