Benzoic acid, 5-[[(2-carboxyphenyl)amino]sulfonyl]-2-chloro-

Base Information

• Chemical Name: Benzoic acid, 5-[[(2-carboxyphenyl)amino]sulfonyl]-2-chloro-
• CAS No.: 91-36-1
• Molecular Formula: C14H10 Cl N O6 S
• Molecular Weight: 355.7503
• European Community (EC) Number: 202-064-7
• UNII: GG4YX75MUN
• DSSTox Substance ID: DTXSID1059024
• Nikkaji Number: J87.256C
• Wikidata: Q81988643
• Mol file: 91-36-1.mol

Synonyms:91-36-1;Benzoic acid, 5-[[(2-carboxyphenyl)amino]sulfonyl]-2-chloro-;EINECS 202-064-7;5-(((2-Carboxyphenyl)amino)sulphonyl)-2-chlorobenzoic acid;Benzoic acid, 5-(((2-carboxyphenyl)amino)sulfonyl)-2-chloro-;5-[(2-carboxyphenyl)sulfamoyl]-2-chlorobenzoic acid;5-[[(2-CARBOXYPHENYL)AMINO]SULPHONYL]-2-CHLOROBENZOIC ACID;GG4YX75MUN;C14H10ClNO6S;DTXSID1059024;C14-H10-Cl-N-O6-S;2-Chloro-5-[(2-carboxyanilino)sulfonyl]benzoic acid;N-[(3-Carboxy-4-chlorophenyl)sulfonyl]anthranilic acid;5-[[(2-Carboxyphenyl)amino]sulfonyl]-2-chlorobenzoic acid

Chemical Property of Benzoic acid, 5-[[(2-carboxyphenyl)amino]sulfonyl]-2-chloro-

Chemical Property:

• Vapor Pressure: 2.14E-15mmHg at 25°C
• Boiling Point: 603.1°C at 760 mmHg
• Flash Point: 318.5°C
• PSA: 129.15000
• Density: 1.65g/cm³
• LogP: 3.69100
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 354.9917359
• Heavy Atom Count: 23
• Complexity: 560

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C(=O)O)NS(=O)(=O)C2=CC(=C(C=C2)Cl)C(=O)O

Refernces

Versatile strategy for oligonucleotide derivatization. Introduction of lanthanide(III) chelates to oligonucleotides

10.1021/ol016093m

2'-Deoxy-5'-O-(4,4'-dimethoxytrityl)uridine (1) is a protected nucleoside, specifically a protected deoxyuridine. The 5'-hydroxyl group is protected with a 4,4'-dimethoxytrityl (DMT) group, which is commonly used in solid phase oligonucleotide synthesis to prevent unwanted reactions at the 5' position. It serves as a starting material for the synthesis of nucleoside phosphoramidite building blocks. The DMT group can be removed later in the synthesis to allow for further functionalization. 2-Cyanoethyl N,N,N',N'-tetraisopropylphosphoramidite is a phosphoramidite reagent used in the phosphorylation step of nucleoside phosphoramidite synthesis. It is used to convert nucleoside derivatives (2a-d) into the desired phosphoramidites (3a-d) which are then used in machine-assisted DNA synthesis. Succinic anhydride, a cyclic anhydride used for alcohol esterification, was used to convert the nucleoside derivative 2a to the corresponding succinate ester (17), which was then immobilized on a long-chain alkylamine CPG polymer support.

Post a RFQ

Cas No.:

Product Name:

Quantity:

Please select Metric Ton KG G Pound L ML

Email:

Company name:

Valid Period:

Detailed Requirements:

• Sample
• MOQ
• GMP
• FDA
• Price
  FOB CIF CFR EXW
• Urgent purchase

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

Remove

Submit

1

What can I do for you?
Get Best Price

Get Best Price for 91-36-1 5-[[(2-carboxyphenyl)amino]sulphonyl]-2-chlorobenzoic acid

Send

Send

Metric Ton KG G Pound L ML

Send

Send