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Naphtho[2,1-b]thiophen-1(2H)-one is a heterocyclic organic compound with the molecular formula C10H6OS. It features a naphthalene core fused with a thiophene ring, and it contains a ketone functional group at the 1-position. Naphtho[2,1-b]thiophen-1(2H)-one is known for its potential applications in the synthesis of various organic compounds and materials, such as pharmaceuticals and dyes, due to its unique structure and reactivity. The presence of both aromatic and sulfur-containing moieties in its structure makes it an interesting candidate for further chemical modifications and exploration in various fields of chemistry.

82-60-0

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82-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82-60-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82-60:
(4*8)+(3*2)+(2*6)+(1*0)=50
50 % 10 = 0
So 82-60-0 is a valid CAS Registry Number.

82-60-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[e][1]benzothiol-1-one

1.2 Other means of identification

Product number -
Other names naphtho[2,1-b]thiophen-1-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82-60-0 SDS

82-60-0Downstream Products

82-60-0Relevant academic research and scientific papers

Integrated Synthesis of Thienyl Thioethers and Thieno[3,2-b]thiophenes via 1-Benzothiophen-3(2 H)-ones

Mitsudo, Koichi,Habara, Nanae,Kobashi, Yoshiaki,Kurimoto, Yuji,Mandai, Hiroki,Suga, Seiji

supporting information, p. 1947 - 1952 (2020/10/06)

A one-pot procedure for the synthesis of thienyl thioethers is described. Several thienyl thioethers were synthesized by a TfOH-promoted Friedel-Crafts-type cyclization, a subsequent nucleophilic attack by an arenethiol, and dehydration. This protocol was

Application of directed metalation in synthesis. Part 8: Interesting example of chemoselectivity in the synthesis of thioaurones and hydroxy ketones and a novel anionic ortho-Fries rearrangement used as a tool in the synthesis of thienopyranones and thiafluorenones

Pradhan, Tarun Kanti,De, Asish,Mortier, Jacques

, p. 9007 - 9017 (2007/10/03)

Chemoselective synthesis of thioaurones or 3-hydroxy benzo[b]thiophen-2- aryl ketones, 1-hydroxy naphtho[2,1-b]thiophen-2-aryl ketones and chalcones from N,N-diethyl-ortho-methyl sulfanyl aryl amides were described. (Benzo[b]thiophen-2-yl) alkylates and (naphtho[2,1-b]thiophen-2-yl) alkylates undergo a novel anionic ortho-Fries rearrangement leading to (3-hydroxy benzo[b]thiophen-2-yl) and (1-hydroxy naphtho[2,1-b]thiophen-2-yl) alkyl ketones. The hydroxy ketones were used as intermediates in the synthesis of wide range of benzothienopyranones and thiafluorenones.

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