2-(Thiophene-2-sulfonamido)acetic acid

Base Information

• Chemical Name: 2-(Thiophene-2-sulfonamido)acetic acid
• CAS No.: 82068-09-5
• Molecular Formula: C₆H₇NO₄S₂
• Molecular Weight: 221.258
• Hs Code.: 2935009090
• DSSTox Substance ID: DTXSID40390058
• Wikidata: Q82186456
• Mol file: 82068-09-5.mol

Synonyms:2-(thiophene-2-sulfonamido)acetic acid;82068-09-5;(Thiophene-2-sulfonylamino)-acetic acid;2-(thiophen-2-ylsulfonylamino)acetic acid;N-(2-THIENYLSULFONYL)GLYCINE;[(thien-2-ylsulfonyl)amino]acetic acid;N-(thiophen-2-ylsulfonyl)glycine;SCHEMBL12465590;DTXSID40390058;UFLYUBNAUREKFD-UHFFFAOYSA-N;HMS1698A12;BBL005603;MFCD03452534;STK863156;[(2-thienylsulfonyl)amino]acetic acid;2-(thiophene-2-sulfonamido)aceticacid;AKOS000126733;(Thiophene-2-sulfonylamino)-aceticacid;SDCCGMLS-0065565.P001;NCGC00336805-01;VS-01585;CS-0247283;EU-0066050;EN300-36291;AB01330748-02;A864463;AQ-390/42133048;SR-01000592757;[(thien-2-ylsulfonyl)amino]acetic acid, AldrichCPR;J-502694;SR-01000592757-1;Z45658540;F1414-0629

Chemical Property of 2-(Thiophene-2-sulfonamido)acetic acid

Chemical Property:

• Vapor Pressure: 7.89E-09mmHg at 25°C
• Boiling Point: 448.5°C at 760 mmHg
• Flash Point: 225°C
• PSA: 120.09000
• Density: 1.573g/cm³
• LogP: 1.58270
• XLogP3: 0.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 220.98165005
• Heavy Atom Count: 13
• Complexity: 282

Purity/Quality:

97% ^*data from raw suppliers

2-(Thiophene-2-sulfonamido)aceticAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CSC(=C1)S(=O)(=O)NCC(=O)O

Technology Process of 2-(Thiophene-2-sulfonamido)acetic acid

There total 1 articles about 2-(Thiophene-2-sulfonamido)acetic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

thiophene-2-sulfonyl chloride (16629-19-9) + glycine (56-40-6,18875-39-3,25718-94-9) → 2-(thiophene-2-sulfonamido)acetic acid (82068-09-5)

Guidance literature:

With sodium hydrogencarbonate; In water; acetone; at 20 ℃;

DOI:10.1016/S0223-5234(00)00127-6

Reference yield: 29.7%

(S)-N-[[3-[3-fluoro-4-(1-piperazinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (154590-66-6,154590-43-9) + 2-(thiophene-2-sulfonamido)acetic acid (82068-09-5) → (S)-N-[[3-[3-fluoro-4-[4-[2-(thiophene-2-sulfonamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide (1160366-95-9)

Guidance literature:

With dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1002/ardp.200800233

Reference yield:

2-(thiophene-2-sulfonamido)acetic acid (82068-09-5) → 2-[benzyl-(thiophene-2-sulfonyl)-amino]-N-hydroxy-acetamide

Guidance literature:

Multi-step reaction with 2 steps

1: Et₃N / acetonitrile / 2 h / Heating

2: NH₂OH*HCl; diisopropylcarbodiimide; Et₃N / acetonitrile / 12 h / 4 °C

With hydroxylamine hydrochloride; triethylamine; diisopropyl-carbodiimide; In acetonitrile; 1: Alkylation / 2: Substitution;

DOI:10.1016/S0223-5234(00)00127-6

upstream raw materials:

thiophene-2-sulfonyl chloride

glycine

Downstream raw materials:

(S)-N-[[3-[3-fluoro-4-[4-[2-(thiophene-2-sulfonamido)acetyl]piperazin-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide

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