1610793-27-5

Basic information

• Product Name: diphenyl (benzo[d]thiazol-5-ylamino)(2-cyclopropylpyrimidin-4-yl)methylphosphonate
• Synonyms: diphenyl (benzo[d]thiazol-5-ylamino)(2-cyclopropylpyrimidin-4-yl)methylphosphonate
• CAS NO: 1610793-27-5
• Molecular Weight: 514.544
• Mol File: 1610793-27-5.mol

Chemical Properties

• CAS DataBase Reference: diphenyl (benzo[d]thiazol-5-ylamino)(2-cyclopropylpyrimidin-4-yl)methylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diphenyl (benzo[d]thiazol-5-ylamino)(2-cyclopropylpyrimidin-4-yl)methylphosphonate(1610793-27-5)
• EPA Substance Registry System: diphenyl (benzo[d]thiazol-5-ylamino)(2-cyclopropylpyrimidin-4-yl)methylphosphonate(1610793-27-5)

Safety Data

• Hazardous Substances Data: 1610793-27-5(Hazardous Substances Data)

Upstream product

• 914348-07-5 2-cyclopropyl-4-(dimethoxymethyl)pyrimidine 
• 1123-93-9 5-aminobenzothiazole 
• 4712-55-4 diphenyl hydrogen phosphite 
• 948549-81-3 2-cyclopropyl pyrimidine 4-carbaldehyde 

Relevant articles and documents

Protonated trititanate nanotubes: an efficient catalyst for one-pot three-component coupling of benzothiazole amines, heterocyclic aldehydes, and dialkyl/diaryl phosphites with a greener perspective

Nano-size catalysts of TiO2, ZnO, CuO, and protonated trititanate nanotubes (H2Ti3O7) have been investigated for the one-pot three component synthesis of novel α-aminophosphonates from benzothiazole amines, hete

Phosphomolybdic acid promoted Kabachnik-Fields reaction: An efficient one-pot synthesis of α-aminophosphonates from 2-cyclopropylpyrimidine-4- carbaldehyde

2-Cyclopropylpyrimidin-4-yl-aryl/benzothiazole derived α- aminophosphonates were synthesized in a simple and efficient method from a three-component condensation reaction of 2-cyclopropylpyrimidin-4-carbaldehyde, various anilines/benzothiazole amines, and different phosphites by using 0.5 mol % of phosphomolybdic acid (PMA, H3PMo12O40) in dichloromethane at room temperature in good to excellent yields with short reaction times.