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3-Thiophenecarbonitrile, 2-amino-4-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

86604-40-2

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86604-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86604-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86604-40:
(7*8)+(6*6)+(5*6)+(4*0)+(3*4)+(2*4)+(1*0)=142
142 % 10 = 2
So 86604-40-2 is a valid CAS Registry Number.

86604-40-2SDS

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 2-amino-4-(4-methoxyphenyl)thiophene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-Thiophenecarbonitrile,2-amino-4-(4-methoxyphenyl)

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:86604-40-2 SDS

86604-40-2Relevant academic research and scientific papers

Synthesis of thieno[2,3-b]quinolinone derivatives

Han, Guang-Fan,Wang, Ming,Chen, Li-Zhuang,Hu, Xiao-Lei

, p. 909 - 912 (2012/10/29)

The Knoevenagel reactions of malononitrile with acetophenone or 4-substituted acetophenons were carried to give the corresponding 2-(1-aryle thylidene)malononitriles, which was further cyclized with sulfur using NaHCO3 as catalysts to generate

Synthesis of substituted amino-cycloalkyl[b]thieno-[3,2-e]pyridines

Seek, Pierre,Thomae, David,Kirsch, Gilbert

, p. 853 - 857 (2008/09/21)

(Chemical Equation Presented) An efficient two respectively three steps procedure for the synthesis of cycloalkyl[b]thieno[3,2-e]-pyridine amines was developed and in general good to very good yields were obtained.

New conditions for the synthesis of thiophenes via the Knoevenagel/Gewald reaction sequence. Application to the synthesis of a multitargeted kinase inhibitor

Barnes, David M.,Haight, Anthony R.,Hameury, Thomas,McLaughlin, Maureen A.,Mei, Jianzhang,Tedrow, Jason S.,Riva Toma, Joan Dalla

, p. 11311 - 11319 (2007/10/03)

Novel conditions have been developed for the preparation of substituted 2-aminothiophenes employing the Knoevenagel condensation followed by the Gewald reaction. The benefits of these conditions are their mildness, and the ease of product isolation. Thus,

Synthesis of polyfunctionally substituted thiophene, thieno[2,3-b]pyridine and thieno[2,3-d]pyrimidine derivatives

Wardakhan, Wagnat W.,Shams, Hoda Z.,Moustafa, Hosam E.

, p. 1815 - 1827 (2007/10/03)

The thiophne derivatives 4a-c were prepared according to the Gewald procedure. Their reactivity towards a variety of chemical reagents was studied to give thienopyridines and pyrimidines. Biological investigations were carried on the newly synthesized pro

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