5-Methyl-1-benzothiophene-2-sulfonyl chloride

Base Information

• Chemical Name: 5-Methyl-1-benzothiophene-2-sulfonyl chloride
• CAS No.: 90273-30-6
• Molecular Formula: C₉H₇ClO₂S₂
• Molecular Weight: 246.738
• Hs Code.: 2934999090
• DSSTox Substance ID: DTXSID70383397
• Wikidata: Q82175090
• Mol file: 90273-30-6.mol

Synonyms:90273-30-6;5-methyl-1-benzothiophene-2-sulfonyl chloride;5-Methylbenzo[b]thiophene-2-sulfonyl chloride;5-Methylbenzo[b]thiophene-2-sulphonyl chloride;5-methylbenzothiophene-2-sulfonyl Chloride;Benzo[b]thiophene-2-sulfonyl chloride, 5-methyl-;SCHEMBL787824;DTXSID70383397;YGGJYXHTCDQVDB-UHFFFAOYSA-N;MFCD06200880;AKOS006220928;PS-10863;5-methyl-benzo[b]thiophenesulfonyl chloride;5-methyl-benzothiophene-2-sulfonyl chloride;CS-0319158;FT-0723689;5-methyl-1-benzothiophene-2-sulfonyl chloride, AldrichCPR;(3S,5S)-5-{(1S,3S)-1-Azido-3-[4- methoxy-3-(3-methoxypropoxy)benzyl]-4-methylpentyl}-3-(propan-2-yl)dihydrofuran-2(3H)-one

Chemical Property of 5-Methyl-1-benzothiophene-2-sulfonyl chloride

Chemical Property:

• Vapor Pressure: 1.03E-05mmHg at 25°C
• Melting Point: 83-84掳C
• Refractive Index: 1.652
• Boiling Point: 382.6°Cat760mmHg
• Flash Point: 185.2°C
• PSA: 70.76000
• Density: 1.486g/cm³
• LogP: 4.21800
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 245.9575995
• Heavy Atom Count: 14
• Complexity: 309

Purity/Quality:

98%Min ^*data from raw suppliers

5-Methylbenzo[b]thiophene-2-sulfonyl chloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C,Xi
• Statements: 36
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC2=C(C=C1)SC(=C2)S(=O)(=O)Cl

Technology Process of 5-Methyl-1-benzothiophene-2-sulfonyl chloride

There total 1 articles about 5-Methyl-1-benzothiophene-2-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:

→ 5-Methylbenzo[b]thiophene-2-sulfonyl chloride (90273-30-6)

Guidance literature:

5-Methylthionaphthen, 1)konz.H2SO4, Ac2O, <20grad (-> Sulfonsaeure; Isolierung als K-Salz) 2)PCl5 (neben 5-Methyl-3(oder 2)-acetylthionaphthen);

DOI:10.1007/BF00918624

Refernces

• 1、 -. "SUBSTITUTED SULFONIC ACID N-[(AMINOIMINOMETHYL)PHENYLALKYL]-AZAHETEROCYCLAMIDE COMPOUNDS". . . Retrieved 2008/06/13.