175137-03-8

Basic information

• Product Name: METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE
• Synonyms: TIMTEC-BB SBB005524;METHYL 3-AMINO-5-[4-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE];METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE;BUTTPARK 37\18-32;3-(Methylamino)-1-butanol
• CAS NO: 175137-03-8
• Molecular Formula: C₁₀H₁₅NO₂S
• Molecular Weight: 213.3
• Mol File: 175137-03-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 94 °C
• Boiling Point: 341.8 °C at 760 mmHg
• Flash Point: 160.5 °C
• Appearance: /
• Density: 1.148g/cm³
• Vapor Pressure: 7.87E-05mmHg at 25°C
• Refractive Index: 1.548
• Storage Temp.: 2-8°C
• CAS DataBase Reference: METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE(175137-03-8)
• EPA Substance Registry System: METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE(175137-03-8)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 24/25
• Hazardous Substances Data: 175137-03-8(Hazardous Substances Data)

Usage

General Description

Methyl 3-amino-5-(tert-butyl)thiophene-2-carboxylate is a chemical compound with the molecular formula C11H15NO2S. It is a thiophene-based molecule containing a tert-butyl group and a carboxylate ester functional group. METHYL 3-AMINO-5-(TERT-BUTYL)THIOPHENE-2-CARBOXYLATE is mainly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active compounds. Its unique structure and reactivity make it a valuable intermediate in the development of new pharmaceuticals and agrochemicals. Additionally, it has shown potential in the field of material science for the production of advanced polymers and materials.

InChI:InChI=1/C10H15NO2S/c1-10(2,3)7-5-6(11)8(14-7)9(12)13-4/h5H,11H2,1-4H3

Upstream product

• 4302-24-3 3-chloro-4,4-dimethylpent-2-enal 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 2365-48-2 Methyl thioglycolate 
• 216574-58-2 3-chloro-4,4-dimethylpent-2-enenitrile 

Downstream Products

• 75782-77-3 3-amino-5-(1,1-dimethylethyl)thiophene hydrochloride 
• 216574-50-4 methyl 3-(N-carbobenzyloxyamino)-5-tert-butylthiophene-2-carboxylate 
• 216574-51-5 N-methyl-3-(N-carbobenzyloxyamino)-5-tert-butylthiophene-2-carboxamide 
• 216573-01-2 5-tert-Butyl-3-(3-p-tolyl-ureido)-thiophene-2-carboxylic acid methyl ester 
• 227623-30-5 N-(5-tert-butyl-thien-3-yl)-N'-(2,3-dichlorophenyl)urea 
• 746671-67-0 3-amino-5-tert-butyl-2-thiophenecarboxylic acid 
• 439692-54-3 6-tert-butyl-4-oxothieno[2,3-d]pyrimidine 
• 439692-55-4 6-tert-butyl-4-chlorothieno[2,3-d]pyrimidine 
• 229003-12-7 N-(5-tert-butyl-2-carboxy-3-thienyl)-N'-(4-(4-pyridinylmethyl)phenyl)-urea 
• 216574-52-6 N-methyl-3-amino-5-tert-butylthiophene-2-carboxamide 

Relevant articles and documents

Synthesis of new thieno[b]azepinediones from α-methylene ketones

New substituted 6,7-dihydro-4H-thieno[3,2-b]azepine-5,8-diones were synthesized in seven steps, starting from substituted α-methylene ketones, via 3-aminothiophene-2-carboxylic acid alkyl esters.