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18159-23-4

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18159-23-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18159-23-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,5 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18159-23:
(7*1)+(6*8)+(5*1)+(4*5)+(3*9)+(2*2)+(1*3)=114
114 % 10 = 4
So 18159-23-4 is a valid CAS Registry Number.

18159-23-4SDS

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 methyl 1-benzylpyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1-benzylpyrrole-2-carboxylic acid methyl ester

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:18159-23-4 SDS

18159-23-4Relevant articles and documents

Design and synthesis of non-peptide mimetics mapping the immunodominant myelin basic protein (MBP83-96) epitope to function as T-cell receptor antagonists

Yannakakis, Mary-Patricia,Simal, Carmen,Tzoupis, Haralambos,Rodi, Maria,Dargahi, Narges,Prakash, Monica,Mouzaki, Athanasia,Platts, James A.,Apostolopoulos, Vasso,Tselios, Theodore V.

, (2017/06/19)

Encephalitogenic T cells are heavily implicated in the pathogenesis of multiple sclerosis (MS), an autoimmune demyelinating disease of the central nervous system. Their stimulation is triggered by the formation of a trimolecular complex between the human

Palladium-Catalyzed Regioselective Dehydrogenative C–H/C–H Cross-Coupling of Pyrroles and Pyridine N-Oxides

Liu, Shanshan,Tzschucke, C. Christoph

supporting information, p. 3509 - 3513 (2016/07/28)

The palladium-catalyzed cross-dehydrogenative coupling of N-alkylpyrroles and pyridine N-oxides gave the corresponding pyrrolylpyridine N-oxides. Cu(OAc)2·H2O as a co-catalyst with air as the terminal oxidant led to preferential coupling in the β-position, whereas AgOAc as the stoichiometric oxidant resulted in preferential coupling in the α-position. N-(Benzyloxymethyl)pyrrole derivatives were deprotected by hydrogenolysis followed by basic hydrolysis.

Synthesis of 2-(N-benzylpyrrolyl)-benzimidazoles using polyphosphoric acid prompted cyclocondensation

Mochona, Bereket,Le, Laine,Gangapuram, Madhavi,Mateeva, Nelly,Ardley, Tiffany,Redda, Kinfe K.

experimental part, p. 1367 - 1371 (2010/12/29)

Synthesis of a series of 2-substituted benzimidazoles was carried out for screening anti-inflammatory activities. 2-(N-benzylpyrrolyl)-benzimidazoles 9a-k were synthesized from N-benzyl-2-pyrrole carboxylic acids 8a-d and 4-substituted-1,2-phenylenediamin

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