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2H-Pyrrole, 3,4-dihydro-3,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87774-48-9

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87774-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87774-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87774-48:
(7*8)+(6*7)+(5*7)+(4*7)+(3*4)+(2*4)+(1*8)=189
189 % 10 = 9
So 87774-48-9 is a valid CAS Registry Number.

87774-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diphenyl-3,4-dihydro-2H-pyrrole

1.2 Other means of identification

Product number -
Other names 2H-Pyrrole,3,4-dihydro-3,5-diphenyl

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:87774-48-9 SDS

87774-48-9Relevant academic research and scientific papers

Construction of 1-pyrroline skeletons by Lewis acid-mediated conjugate addition of vinyl azides

Zhu, Xu,Chiba, Shunsuke

supporting information, p. 2473 - 2476 (2016/02/18)

Lewis acid-mediated conjugate addition of vinyl azides to electron-deficient alkenes led to the efficient construction of 1-pyrroline skeletons. The reactions of vinyl azides with 3-alkylidene-2-oxoindolines afford 3′,4′-dihydrospiro[indoline-3,2′-pyrrol]-2-ones in a diastereoselective fashion, whereas those with dimethyl 2-alkylidenemalonates provide 4,5-dihydro-3H-pyrroles.

Δ1-pyrroline based boranyls: Synthesis, crystal structures and luminescent properties

Cardona, Francisco,Rocha, Jo?o,Silva, Artur M.S.,Guieu, Samuel

, p. 16 - 20 (2014/06/24)

Two new Δ1-pyrroline ligands and their corresponding boron complexes have been synthesized and characterized. Their luminescent properties were investigated, the boron complexes emitting brightly around 410 nm. The presence of the exocyclic dou

A facile synthesis of isoindoline and Δ1-pyrrolines from chalcone and glycine by a cascade of process involving addition, in situ decarboxylation, and cyclization

Elamparuthi, Elangovan,Sarathkumar, Subramaniayan,Girija, Swaminathan,Anbazhagan, Veerappan

supporting information, p. 3992 - 3995 (2014/07/08)

In this Letter, we report a rapid one-step entry into isoindoline and Δ1-pyrrolines from chalcone. The key step in the synthesis is the addition of glycine to chalcone. In acidic medium the reaction presumably goes through aza-Michael addition,

One-pot synthesis of substituted Δ1-pyrrolines through the Michael addition of nitroalkanes to chalcones and subsequent reductive cyclization in aqueous media

Liang, Yongjiu,Dong, Dewen,Lu, Yumei,Wang, Yan,Pan, Wei,Chai, Yanyan,Liu, Qun

, p. 3301 - 3304 (2008/09/17)

A facile and efficient one-pot synthesis of substituted Δ1-pyrrolines in aqueous media has been developed. Upon treatment with aqueous sodium hydroxide in N,N-dimethylformamide, a range of chalcones underwent room temperature Michael addition r

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