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19137-96-3

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19137-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19137-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,3 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19137-96:
(7*1)+(6*9)+(5*1)+(4*3)+(3*7)+(2*9)+(1*6)=123
123 % 10 = 3
So 19137-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H20N2/c1-2-7-15(8-3-1)14-21-12-6-11-19(21)17-13-20-18-10-5-4-9-16(17)18/h1-5,7-10,13,19-20H,6,11-12,14H2

19137-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-benzylpyrrolidin-2-yl)-1H-indole

1.2 Other means of identification

Product number -
Other names 3-(1-Benzyl-2-pyrrolidinyl)indole

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:19137-96-3 SDS

19137-96-3Downstream Products

19137-96-3Relevant articles and documents

Condensations based on 5-(indol-3-yl)-pyrrolidin-2-thiones

Sadovoy, Andrey V.,Kattsyna, Veronica V.,Protopopova, Polina S.,Nelyubina, Yulia V.,Pavlov, Alexander A.,Kochetkov, Konstantin A.,Sviridova, Lyudmila A.

, (2018/11/25)

New activated indolylpyrrolidones—their methylthiopyrrolinium salts—in the reactions with several CH-acids were studied. 2-Nitromethylene- and 2-dicyanomethyleneindolylpyrrolidines were obtained from 5-indolyl-2-methylthiopyrrolinium salts with good yields. The reduction in these nitro compounds yields the respective aminomethylpyrolidines. The rigid structure of the starting compounds has significant stereoelectronic requirements of nucleophilic agents.

Biomimetic Approach toward the Total Synthesis of rac-2-(Acylmethylene)pyrrolidine Alkaloids

Shih, Yu-Chiao,Tsai, Pei-Hua,Hsu, Chia-Chun,Chang, Chih-Wei,Jhong, Yuandong,Chen, Yun-Chung,Chien, Tun-Cheng

, p. 6669 - 6678 (2015/10/06)

2-(Acylmethylene)pyrrolidine derivatives were synthesized via intermolecular decarbonylative Mannich reaction from various methyl ketones and 1-alkyl-1-pyrroliniums, generated in situ from 1-alkylprolines. This approach mimics the biosynthetic pathway and provides a direct access to a series of 2-(acylmethylene)pyrrolidine alkaloids, including hygrine, N-methylruspolinone, dehydrodarlinine, and ruspolinone.

Synthesis and pharmacological activity of 3-(2-pyrrolidinyl)indoles

Youngdale et al.

, p. 415,424 (2007/10/05)

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