3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid

Base Information

• Chemical Name: 3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid
• CAS No.: 408360-05-4
• Molecular Formula: C11H13 N O4 S2
• Molecular Weight: 287.361
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID90389376
• ChEMBL ID: CHEMBL1375878
• Mol file: 408360-05-4.mol

Synonyms:408360-05-4;3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid;3-Tosylthiazolidine-2-carboxylic acid;3-(4-methylphenyl)sulfonyl-1,3-thiazolidine-2-carboxylic acid;BAS 00608459;SMR000123021;Oprea1_265525;Oprea1_421933;MLS000035478;CHEMBL1375878;DTXSID90389376;HMS1697O07;HMS2418G16;3-[(4-methylphenyl)sulfonyl]-1,3-thiazolidine-2-carboxylic acid;3-Tosylthiazolidine-2-carboxylicacid;STK092276;AKOS000580773;AKOS022084805;CS-0332388;A923353;SR-01000312581;SR-01000312581-1;3-(TOLUENE-4-SULFONYL)-THIAZOLIDINE-2-CARBOXYLICACID;3-(toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid, AldrichCPR

Chemical Property of 3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid

Chemical Property:

• Vapor Pressure: 1.43E-11mmHg at 25°C
• Boiling Point: 518.4°Cat760mmHg
• Flash Point: 267.3°C
• PSA: 108.36000
• Density: g/cm³
• LogP: 2.16190
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 287.02860024
• Heavy Atom Count: 18
• Complexity: 409

Purity/Quality:

97% ^*data from raw suppliers

3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi,T
• Statements: 25
• Safety Statements: 45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)S(=O)(=O)N2CCSC2C(=O)O

Technology Process of 3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic acid

There total 1 articles about 3-(Toluene-4-sulfonyl)-thiazolidine-2-carboxylic 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:

C13H17NO4S2 (1265898-58-5) → C11H13NO4S2 (408360-05-4)

Guidance literature:

With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 4h;

DOI:10.1016/j.bmcl.2010.10.123

Reference yield:

4-amino-tricyclo[3,3,1,13,7]decane-1-carboxamide (1222495-90-0) + C11H13NO4S2 (408360-05-4) → C22H29N3O4S2 (1265898-49-4)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; isopropyl alcohol; at 20 ℃; for 5h;

DOI:10.1016/j.bmcl.2010.10.123

upstream raw materials:

C₁₃H₁₇NO₄S₂

Downstream raw materials:

C₂₂H₂₉N₃O₄S₂

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