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2-(1H-INDOL-3-YL)-2-THIEN-2-YLETHANAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51626-50-7

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51626-50-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51626-50-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,2 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51626-50:
(7*5)+(6*1)+(5*6)+(4*2)+(3*6)+(2*5)+(1*0)=107
107 % 10 = 7
So 51626-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2S/c15-8-11(14-6-3-7-17-14)12-9-16-13-5-2-1-4-10(12)13/h1-7,9,11,16H,8,15H2/p+1/t11-/m0/s1

51626-50-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-indol-3-yl)-2-thiophen-2-ylethanamine

1.2 Other means of identification

Product number -
Other names BB_SC-3619

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:51626-50-7 SDS

51626-50-7Relevant academic research and scientific papers

Friedel-Crafts alkylation reaction with fluorinated alcohols as hydrogen-bond donors and solvents

Tang, Ren-Jin,Milcent, Thierry,Crousse, Benoit

, p. 10314 - 10317 (2018/03/26)

An effective and clean FC alkylation of indoles and electron-rich arenes with β-nitroalkenes in HFIP was reported. The desired products are formed rapidly in excellent yields under mild conditions without the need for any additional catalysts or reagents. Further, this methodology can be applied to one-pot synthesis of biologically active tryptamine derivatives.

Use of the Pictet-Spengler reaction for the synthesis of 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines and 1,4-disubstituted-β-carbolines: formation of γ-carbolines

Kusurkar, Radhika S.,Alkobati, Nabil A.H.,Gokule, Anita S.,Puranik, Vedavati G.

, p. 1654 - 1662 (2008/09/17)

Microwave-assisted conjugate addition of indole on nitro-olefins furnished nitro compounds, which were reduced to tryptamines. Further, by using Pictet-Spengler condensation, new 1,4-disubstituted-1,2,3,4-tetrahydro-β-carbolines were synthesized in diaste

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