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Pyrrolidine, 2-butyl-5-heptyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61772-92-7

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61772-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61772-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,7 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61772-92:
(7*6)+(6*1)+(5*7)+(4*7)+(3*2)+(2*9)+(1*2)=137
137 % 10 = 7
So 61772-92-7 is a valid CAS Registry Number.

61772-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butyl-5-heptylpyrrolidine

1.2 Other means of identification

Product number -
Other names Pyrrolidine,2-butyl-5-heptyl

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:61772-92-7 SDS

61772-92-7Downstream Products

61772-92-7Relevant academic research and scientific papers

Reaction of Nitrogen-Radicals with Organometallics Under Ni-Catalysis: N-Arylations and Amino-Functionalization Cascades

Angelini, Lucrezia,Davies, Jacob,Simonetti, Marco,Malet Sanz, Laia,Sheikh, Nadeem S.,Leonori, Daniele

, p. 5003 - 5007 (2019/03/17)

Herein, we report a strategy for the generation of nitrogen-radicals by ground-state single electron transfer with organyl–NiI species. Depending on the philicity of the N-radical, two types of processes have been developed. In the case of nucleophilic aminyl radicals direct N-arylation with aryl organozinc, organoboron, and organosilicon reagents was achieved. In the case of electrophilic amidyl radicals, cascade processes involving intramolecular cyclization, followed by reaction with both aryl and alkyl organometallics have been developed. The N-cyclization–alkylation cascade introduces a novel retrosynthetic disconnection for the assembly of substituted lactams and pyrrolidines with its potential demonstrated in the short total synthesis of four venom alkaloids.

A NEW SYNTHETHIC ASPECT OF ACETIC NITRONIC ANHYDRIDES

Miyashita, Masaaki,Awen, Bahlul Z. E.,Yoshikoshi, Akira

, p. 7569 - 7586 (2007/10/02)

A facile and convenient synthesis of acetic nitronic anhydrides from aliphatic nitroalkenes and lithium ketone enolates and the efficient conversion of these anhydrides to 1,4-diketones, alkylpyrroles, diketone monooximes, dihydro-1,2-oxazines, pyrrolidin

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