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S-naphthalen-2-yl 4-nitrobenzenecarbothioate is a chemical compound with the molecular formula C18H11NOS2NO2. It is an organic compound that features a naphthalene ring (a fused pair of benzene rings) at the sulfur end of a thioester linkage, with a 4-nitrobenzene group attached to the carbonyl carbon. S-naphthalen-2-yl 4-nitrobenzenecarbothioate is characterized by its yellow crystalline appearance and is soluble in organic solvents. It is used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a valuable intermediate in the synthesis of certain complex molecules.

6629-65-8

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6629-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6629-65-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6629-65:
(6*6)+(5*6)+(4*2)+(3*9)+(2*6)+(1*5)=118
118 % 10 = 8
So 6629-65-8 is a valid CAS Registry Number.

6629-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name S-naphthalen-2-yl 4-nitrobenzenecarbothioate

1.2 Other means of identification

Product number -
Other names 4-nitro-thiobenzoic acid S-[2]naphthyl ester

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:6629-65-8 SDS

6629-65-8Downstream Products

6629-65-8Relevant academic research and scientific papers

Methanesulfonic anhydride-promoted sustainable synthesis of thioesters from feedstock acids and thiols

Singh, Pallavi,Peddinti, Rama Krishna

, (2021/02/22)

Abstract: An unprecedented metal-, halogen- and solvent-free, MSAA-promoted S-carbonylation of thiols with feedstock acids has been developed. This new transformation provides an efficient and atom-economic strategy for the synthesis of thioesters in a single operation from readily available and inexpensive starting materials. The reaction avoids the use of expensive and hazardous coupling reagents, bases and generates water as the only by-product, thus making this chemical synthetic process more viable, environment-friendly and contributing towards sustainable chemistry. Graphic abstract: [Figure not available: see fulltext.].

TFFH as an excellent reagent for acylation of alcohols, thiols and dithiocarbamates

Pittelkow, Michael,Kamounah, Fadhil S.,Boas, Ulrik,Pedersen, Brian,Christensen, Jorn B.

, p. 2485 - 2492 (2007/10/03)

A convenient and easy procedure to synthesize esters and thioesters from the corresponding carboxylic acid using TFFH as the coupling reagent is described. The preparation of N-acyl-dithiocarbamates from carboxylic acids and 1,3-thiazolidine-2-thione with TFFH as the coupling reagent is also described.

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