53826-78-1

Basic information

• Product Name: METHYL 4-FORMYLAMINOTHIOPHENE-3-CARBOXYLATE
• Synonyms: METHYL 4-FORMYLAMINOTHIOPHENE-3-CARBOXYLATE
• CAS NO: 53826-78-1
• Molecular Formula: C₇H₇NO₃S
• Molecular Weight: 185.2
• Mol File: 53826-78-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: METHYL 4-FORMYLAMINOTHIOPHENE-3-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 4-FORMYLAMINOTHIOPHENE-3-CARBOXYLATE(53826-78-1)
• EPA Substance Registry System: METHYL 4-FORMYLAMINOTHIOPHENE-3-CARBOXYLATE(53826-78-1)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 53826-78-1(Hazardous Substances Data)

Upstream product

• 39978-14-8 methyl 3-amino-4-thiophenecarboxylate hydrochloride 
• 64-18-6 formic acid 
• 69363-85-5 methyl 4-aminothiophene-3-carboxylate 
• 2689-68-1 methyl 4-oxotetrahydrothiophene-3-carboxylate 
• 2258-42-6 formyl acetic anhydride 

Downstream Products

• 53826-73-6 thieno<3,4-d>pyrimidin-4(3H)-one 
• 108180-63-8 4-((tert-butoxycarbonyl)amino)-3-thiophenecarboxylic acid 
• 161940-20-1 methyl 4-((tert-butoxycarbonyl)amino)thiophene-3-carboxylate 
• 1238578-88-5 C₃₄H₃₅NO₇S 
• 118674-77-4 5-((2S,3R,4R,5R)-3,4-Bis-benzoyloxy-5-benzoyloxymethyl-tetrahydro-furan-2-yl)-4-formylamino-thiophene-3-carboxylic acid methyl ester 
• 118674-65-0 5-((2R,3R,4R,5R)-3,4-Bis-benzoyloxy-5-benzoyloxymethyl-tetrahydro-furan-2-yl)-4-formylamino-thiophene-3-carboxylic acid methyl ester 
• 21585-88-6 3-benzyl-3H-thieno[3,4-d]pyrimidin-4-one 

Relevant articles and documents

Emissive RNA alphabet

A fluorescent ribonucleoside alphabet consisting of highly emissive purine (thA, thG) and pyrimidine (thU, thC) analogues, all derived from thieno[3,4-d]pyrimidine as the heterocyclic nucleus, is described. Stru

Competitive ortho metalation effects: The kinetic and thermodynamic lithiation of 3-(tert-butoxycarbonyl)amino-4-carbomethoxythiophene

Deprotanation of the thiophene 1 under kinetically controlled conditions with LDA takes place next to the NHBoc group and under thermodynamic conditions next to the methyl eater. N-Methylation leads to exclusive lithiation next to the ester. The methylester was found to be superior to the diethylamide in facilitating lithiation.