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Methyl 2-[(2-methoxy-2-oxoethyl)sulfanyl]benzoate is a complex organic chemical compound with the molecular formula C11H12O5S. It is a colorless to pale yellow liquid with a molecular weight of 260.27 g/mol. methyl 2-[(2-methoxy-2-oxoethyl)sulfanyl]benzoate is characterized by the presence of a benzoate group, a sulfanyl group, and a methoxy-oxoethyl group. It is synthesized through a series of chemical reactions and is used in various applications, including pharmaceuticals and agrochemicals, due to its unique chemical properties and reactivity. The compound is also known for its potential as a precursor in the synthesis of other complex molecules.

6287-88-3

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6287-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6287-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6287-88:
(6*6)+(5*2)+(4*8)+(3*7)+(2*8)+(1*8)=123
123 % 10 = 3
So 6287-88-3 is a valid CAS Registry Number.

6287-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-(2-methoxy-2-oxoethyl)sulfanylbenzoate

1.2 Other means of identification

Product number -
Other names Thiosalicylsaeuremethylester-S-essigsaeuremethylester

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:6287-88-3 SDS

6287-88-3Relevant academic research and scientific papers

Efficient synthesis and 5-LOX/COX-inhibitory activity of some 3-hydroxybenzo[b]thiophene-2-carboxylic acid derivatives

Hansen, Finn K.,Khankischpur, Mehdi,Tolaymat, Ibrahim,Mesaros, Renata,Dannhardt, Gerd,Geffken, Detlef

experimental part, p. 5031 - 5034 (2012/08/28)

A series of 3-hydroxybenzo[b]thiophene-2-carboxylic acid derivatives has been prepared and subsequently evaluated with regards to the inhibition of 5-LOX/COX. Structure optimization furnished derivatives with promising in vitro activity as dual 5-LOX/COX inhibitors with submicromolar IC50 values for inhibition of 5-LOX and COX-1, respectively.

A convenient synthesis of benzothiophene derivatives

Cabiddu, M.Grazia,Cabiddu, Salvatore,Cadoni, Enzo,Demontis, Stefania,Fattuoni, Claudia,Melis, Stefana

, p. 4529 - 4533 (2007/10/03)

(Methylthio)- and 2-bromo-1-(methylthio)benzene are useful synthons to prepare monometallated and bimetallated intermediates which lead to 1-benzothiophenes functionalized in the three and/or two positions.

Novel benzothiophene-, benzofuran-, and naphthalenecarboxamidotetrazoles as potential antiallergy agents

Connor,Cetenko,Mullican,Sorenson,Unangst,Weikert,Adolphson,Kennedy,Thueson,Wright,Conroy

, p. 958 - 965 (2007/10/02)

The synthesis and antiallergic activity of a series of novel benzothiophene-, benzofuran-, and naphthalenecarboxamidotetrazoles are described. A number of the compounds inhibit the release of histamine from anti-IgE stimulated basophils obtained from alle

3-Alkoxy-thianapthene-2-carboxamides

-

, (2008/06/13)

The 3-alkoxy-thianaphthene-2-carboxamides of this invention are effective for the treatment of mammals afflicted with emesis. When administered to dogs in dosages of 250 μg/kg, compounds of this invention give 100% protection against vomiting normally induced by subcutaneous administration of apomorphine. The compounds of this invention also favorably modify behavior disturbances in mammals.

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