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N-[7-(benzyloxy)-4-(methylsulfanyl)-3-nitro-4H-2-chromenyl]-N-methylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173429-61-2

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1173429-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173429-61-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,4,2 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1173429-61:
(9*1)+(8*1)+(7*7)+(6*3)+(5*4)+(4*2)+(3*9)+(2*6)+(1*1)=152
152 % 10 = 2
So 1173429-61-2 is a valid CAS Registry Number.

1173429-61-2Downstream Products

1173429-61-2Relevant academic research and scientific papers

Choline hydroxide: An efficient and biodegradable catalyst for the synthesis of 2-amino-3-nitro-4H-chromene derivatives in an aqueous medium

Krishnammagari, Suresh Kumar,Lim, Kwon Taek,Cho, Byung Gwon,Tae Jeong, Yeon

, p. 574 - 581 (2018)

An expedient, eco-friendly and efficient procedure for the synthesis of novel 2-amino-3-nitro-4H-chromene derivatives has been developed through the reaction of various 2-hydroxybenzaldehydes and (E)-N-methyl-1-(methylthio)-2-nitroethenamine in the presence of the basic ionic liquid catalyst (choline hydroxide (ChOH)) at room temperature an aqueous medium. The advantageous of this method is a biodegradable and recyclable catalyst, mild, environmentally friendly and high products yields (83-96%) in short reaction times.

Nitroketene acetal chemistry: efficient synthesis of 2-amino-3-nitro-4H-chromenes

Rao, H. Surya Prakash,Geetha

supporting information; experimental part, p. 3836 - 3839 (2009/10/11)

Base-catalyzed reaction of the nitroketene N,S-acetals and the ring substituted 2-hydroxybenzaldehydes afforded a combinatorial library of the 2-alkylamino-3-nitro-4-alkylsulfanyl 4H-chromenes in excellent yields. Nucleophilic displacement of the C4 alkylsulfanyl group with different thiols afforded 4H-chromenes with structural diversity.

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