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6961-27-9

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6961-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6961-27-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6961-27:
(6*6)+(5*9)+(4*6)+(3*1)+(2*2)+(1*7)=119
119 % 10 = 9
So 6961-27-9 is a valid CAS Registry Number.

6961-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-nitro-1H-indol-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-propanoicacid,5-nitro

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:6961-27-9 SDS

6961-27-9Downstream Products

6961-27-9Relevant articles and documents

Synthesis of CF3-Containing Spirocyclic Indolines via a Red-Light-Mediated Trifluoromethylation/Dearomatization Cascade

Gianetti, Thomas L.,Mei, Liangyong,Moutet, Jules,Stull, Savannah M.

supporting information, p. 10640 - 10653 (2021/07/31)

A red-light-mediated nPr-DMQA+-catalyzed cascade intramolecular trifluoromethylation and dearomatization of indole derivatives with Umemoto's reagent has been developed. This protocol provides a facile and efficient approach for the construction of functionalized and potentially biologically important CF3-containing 3,3-spirocyclic indolines with moderate to high yields and excellent diastereoselectivities under mild conditions. The success of multiple gram-scale (1 and 10 g) experiments further highlights the robustness and practicality of this protocol and the merit of the employment of red light. Mechanistic studies support the formation of a crucial CF3 radical species and a dearomatized benzyl carbocation intermediate.

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