2,3-dihydro-1H-indene-5-sulfonyl chloride

Base Information

• Chemical Name: 2,3-dihydro-1H-indene-5-sulfonyl chloride
• CAS No.: 52205-85-3
• Molecular Formula: C9H9ClO2S
• Molecular Weight: 216.688
• Hs Code.: 2904909090
• European Community (EC) Number: 695-600-8
• DSSTox Substance ID: DTXSID40389745
• Wikidata: Q82185852
• Mol file: 52205-85-3.mol

Synonyms:52205-85-3;indane-5-sulfonyl chloride;2,3-dihydro-1H-indene-5-sulfonyl chloride;Indan-5-sulfonyl chloride;MFCD05237217;indan-5-sulfonylchloride;5-indanesulfonoyl chloride;indane-5-sulphonyl chloride;indan-5-sulfonic acid chloride;SCHEMBL1546679;DTXSID40389745;Indan-5-sulfonyl chloride, 97%;SWLIXMXSCZYVTQ-UHFFFAOYSA-N;BBL013244;STK502248;AKOS000123198;indan-5-sulfonyl chloride, AldrichCPR;AT13425;DB-0800;CS-0208425;FT-0677217;EN300-11191;A808970;A828978;J-506984;Z104502890;3-AMINO-3-(5-METHYL-THIOPHEN-2-YL)-PROPIONICACID

Chemical Property of 2,3-dihydro-1H-indene-5-sulfonyl chloride

Chemical Property:

• Vapor Pressure: 0.000536mmHg at 25°C
• Melting Point: 45-50°C
• Refractive Index: 1.588
• Boiling Point: 322.1°Cat760mmHg
• Flash Point: 148.6°C
• PSA: 42.52000
• Density: 1.396g/cm³
• LogP: 3.18360
• Sensitive.: Moisture Sensitive
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 216.0011784
• Heavy Atom Count: 13
• Complexity: 281

Purity/Quality:

99% ^*data from raw suppliers

Indane-5-sulfonylChloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CC2=C(C1)C=C(C=C2)S(=O)(=O)Cl

Technology Process of 2,3-dihydro-1H-indene-5-sulfonyl chloride

There total 5 articles about 2,3-dihydro-1H-indene-5-sulfonyl chloride 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: 62.0%

→ indan-5-sulfonyl chloride (52205-85-3)

Guidance literature:

Reference yield:

INDANE (496-11-7) → indan-5-sulfonyl chloride (52205-85-3)

Guidance literature:

With chlorosulphuric acid; at -10 ℃;

DOI:10.1021/ja01850a049

Reference yield:

chlorosulfonic acid (7790-94-5) + INDANE (496-11-7) → indan-5-sulfonyl chloride (52205-85-3)

Guidance literature:

In dichloromethane;

upstream raw materials:

INDANE

chlorosulfonic acid

Downstream raw materials:

1-(Indane-5-sulfonyl)-2-methoxy-4-phenyl-4,5-dihydro-1H-imidazole

1-(Indane-5-sulfonyl)-2-methoxy-5-phenyl-4,5-dihydro-1H-imidazole

1-(Indane-5-sulfonyl)-2-methoxy-4-p-tolyl-4,5-dihydro-1H-imidazole

1-(Indane-5-sulfonyl)-2-methoxy-5-p-tolyl-4,5-dihydro-1H-imidazole

Refernces

• 1、 -. "ANTITUMOR BENZOYLSULFONAMIDES". Page 13. . Retrieved 2008/06/13.
• 2、 Bock, Hans,Rittmeyer, Peter. "RADIKALIONEN 89. EINELEKTRONEN-OXIDATIONEN VON DIARYLDISULFIDEN MIT AlCl3/H2CCl2". . p. 261 - 292. Retrieved 2007/10/02.