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2-(Tetrahydrofuran-2-yl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50640-01-2

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50640-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50640-01-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,4 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50640-01:
(7*5)+(6*0)+(5*6)+(4*4)+(3*0)+(2*0)+(1*1)=82
82 % 10 = 2
So 50640-01-2 is a valid CAS Registry Number.

50640-01-2SDS

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 2-tetrahydrofuran-2-yl-indole

1.2 Other means of identification

Product number -
Other names 2-(2'-Tetrahydrofuranyl)indol

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:50640-01-2 SDS

50640-01-2Downstream Products

50640-01-2Relevant academic research and scientific papers

Nickel-Catalyzed Regioselective Cross-Dehydrogenative Coupling of Inactive C(sp3)-H Bonds with Indole Derivatives

Jin, Li-Kun,Wan, Li,Feng, Jie,Cai, Chun

supporting information, p. 4726 - 4729 (2015/10/12)

A nickel-catalyzed regiosepecific C2- versus C3-oxidative cross-coupling reaction of indoles with 1,4-dioxane and other inactive C(sp3)-H bonds is described. The divergent synthesis of C(sp3)-C(sp2) bonds was achieved in satisfactory yields with di-tert-butyl peroxide (DTBP) as the oxidant, which provides an efficient strategy for the selective construction of cyclic ethers containing heteroaromatic core structures.

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