2-(6-Chloro-1H-indol-3-yl)ethanol

Base Information

• Chemical Name: 2-(6-Chloro-1H-indol-3-yl)ethanol
• CAS No.: 41340-35-6
• Molecular Formula: C10H10ClNO
• Molecular Weight: 195.648
• DSSTox Substance ID: DTXSID20520997
• Wikidata: Q82385202
• Mol file: 41340-35-6.mol

Synonyms:2-(6-Chloro-1H-indol-3-yl)ethanol;41340-35-6;2-(6-Chloro-1H-indol-3-yl)ethan-1-ol;SCHEMBL24452687;DTXSID20520997;AKOS006315538;EN300-1982672

Chemical Property of 2-(6-Chloro-1H-indol-3-yl)ethanol

Chemical Property:

• Storage Temp.: 2-8°C
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 195.0450916
• Heavy Atom Count: 13
• Complexity: 176

Purity/Quality:

99% ^*data from raw suppliers

1H-INDOLE-3-ETHANOL,6-CHLORO- 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C(C=C1Cl)NC=C2CCO

Technology Process of 2-(6-Chloro-1H-indol-3-yl)ethanol

There total 2 articles about 2-(6-Chloro-1H-indol-3-yl)ethanol 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:

2-ethoxytetrahydrofuran (13436-46-9) + m-chlorophenylhydrazine hydrochloride (2312-23-4) → 2-(6-chloro-1H-indol-3-yl)ethanol (41340-35-6)

Guidance literature:

In ethanol; Heating;

DOI:10.1021/jm061278q

Reference yield:

2-(3-indole)-ethanol (526-55-6,930395-07-6) → 2-(6-chloro-1H-indol-3-yl)ethanol (41340-35-6)

Guidance literature:

With glucose dehydrogenase; D-glucose; maltose binding protein-rebeccamycin halogenase; rebeccamycin halogenase variant 8F; flavin adenine dinucleotide; NADH; sodium chloride; In isopropyl alcohol; at 10 ℃; pH=7.4; Enzymatic reaction;

DOI:10.1039/c5sc04680g

Reference yield: 99.0%

2-(6-chloro-1H-indol-3-yl)ethanol (41340-35-6) + (E)-diphenyl(3-styryl-1H-indol-2-yl)methanol → 2-(6-chloro-2-(2,3,3-triphenyl-1,2,3,4-tetrahydrocyclopenta[b]indol-1-yl)-1H-indol-3-yl)ethanol

Guidance literature:

With toluene-4-sulfonic acid; In chloroform; at 40 ℃; for 8h; chemoselective reaction;

DOI:10.1021/acs.joc.8b00414

upstream raw materials:

2-ethoxytetrahydrofuran

m-chlorophenylhydrazine hydrochloride

2-(3-indole)-ethanol

Downstream raw materials:

6-chloro-3-(p-toluenesulfonyloxyethyl)-1-(p-toluenesulfonyl)indole

6-chloro-3-(2-iodoethyl)-1-(p-toluenesulfonyl)indole

6-chloro-2-(3''-(6''-chloro-1''-(p-toluenesulfonyl)indolyl)ethyloxy)-3',4',5'-triacetyladenosine

2-(3-(6-chloro-1-(p-toluenesulfonyl)indolyl)ethyloxy)adenosine

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