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Pyrido[1,2-a]benzimidazole,1,2,3,4-tetrahydro-7-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18390-15-3

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18390-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18390-15-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,9 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18390-15:
(7*1)+(6*8)+(5*3)+(4*9)+(3*0)+(2*1)+(1*5)=113
113 % 10 = 3
So 18390-15-3 is a valid CAS Registry Number.

18390-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-1,2,3,4-tetrahydropyrido[1,2-a]benzimidazole

1.2 Other means of identification

Product number -
Other names 7-Methyl-1,2,3,4-tetrahydropyrido<1,2-a>benzimidazol

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:18390-15-3 SDS

18390-15-3Downstream Products

18390-15-3Relevant academic research and scientific papers

Metal-free construction of tricyclic or tetracyclic compounds - Acid-promoted synthesis of benzo[4,5]imidazo[2,1-a]isoindole and 1,2-dialkyl-2,3-dihydrobenzimidazoles

Chen, Jinying,Qu, Jinpeng,Zhang, Yuanqing,Chen, Yongxin,Liu, Na,Chen, Baohua

supporting information, p. 316 - 319 (2013/01/15)

An environmental friendly, efficient, and easy to operate strategy for synthesizing of benzo[4,5]imidazo[2,1-a]isoindole and 1,2-dialkyl-2,3- dihydrobenzimidazoles via acid-promoted coupling of dialdehyde and o-diaminobenzene under metal-free conditions is described. A series of products were generated in good yields under mild conditions.

Reactivity-controlled regioselectivity: A regiospecific synthesis of 1,2-disubstituted benzimidazoles

Deng, Xiaohu,Mani, Neelakandha S.

experimental part, p. 680 - 686 (2010/03/04)

We demonstrate exceptional levels of regioselectivity in the tandem, animation reactions between 1,2-differentiated dihaloarenes and N-substituted amidines, The regiochemical outcome of this Cul-catalyzed reaction is achieved through a combination of N1/N2 chemoselectivity on the amidine and reactivity-controlled X1/X2 chemoselectivity on the 1,2-dihaloarene. This reaction proves to be fairly general for the regiospecific synthesis of 1,2-substituted benzimidazoles.

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