1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy-

Base Information

• Chemical Name: 1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy-
• CAS No.: 126588-10-1
• Molecular Formula: C6H4Cl2O6S2
• Molecular Weight: 307.132
• DSSTox Substance ID: DTXSID00469638
• Wikidata: Q82297449
• Mol file: 126588-10-1.mol

Synonyms:126588-10-1;1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy-;SCHEMBL23747994;DTXSID00469638

Chemical Property of 1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy-

Chemical Property:

• XLogP3: 1.8
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 305.8826356
• Heavy Atom Count: 16
• Complexity: 446

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C=C(C(=C1O)O)S(=O)(=O)Cl)S(=O)(=O)Cl

Technology Process of 1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy-

There total 2 articles about 1,3-Benzenedisulfonyl dichloride, 4,5-dihydroxy- 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:

benzene-1,2-diol (120-80-9,19481-10-8,37349-32-9) → 3,5-bis(dichlorosulfonyl)catechol (126588-10-1)

Guidance literature:

With chlorosulfonic acid; at 110 ℃;

Reference yield:

chlorosulfonic acid (7790-94-5) + benzene-1,2-diol (120-80-9,19481-10-8,37349-32-9) → 3,5-bis(dichlorosulfonyl)catechol (126588-10-1)

Guidance literature:

at 110 ℃;

Reference yield: 78.0%

3,5-bis(dichlorosulfonyl)catechol (126588-10-1) → catechol-3,5-bis-sulphonylhydrazide (76987-28-5)

Guidance literature:

With hydrazine hydrate; In pyridine; at 0 ℃;

upstream raw materials:

benzene-1,2-diol

chlorosulfonic acid

Downstream raw materials:

4,5-Dihydroxy-benzene-1,3-disulfonic acid di-p-tolyl ester

catechol-3,5-bis-sulphonylhydrazide

4,5-Dihydroxy-benzene-1,3-disulfonic acid bis-p-tolylamide

4,5-Dihydroxy-benzene-1,3-disulfonic acid bis-[(4-chloro-phenyl)-amide]

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