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methyl-α-hydroxy-β-[(2-(methoxycarbonyl)ethyl)thio]-2-(8-phenyloctyl)benzenepropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120427-74-9

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120427-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120427-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,2 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120427-74:
(8*1)+(7*2)+(6*0)+(5*4)+(4*2)+(3*7)+(2*7)+(1*4)=89
89 % 10 = 9
So 120427-74-9 is a valid CAS Registry Number.

120427-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl-α-hydroxy-β-[(2-(methoxycarbonyl)ethyl)thio]-2-(8-phenyloctyl)benzenepropanoate

1.2 Other means of identification

Product number -
Other names .Methyl 3-(2-Carbomethoxyethylthio)-3-[2-(8-phenyloctyl)phenyl]-2-hydroxypropionate

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:120427-74-9 SDS

120427-74-9Relevant academic research and scientific papers

Process and intermediate for the preparation of 2-hydroxy-3-sulfido-3-phenyl propanoic acids

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, (2008/06/13)

STR1 This invention relates to intermediate compounds of formula (VI), wherein: R1 is (L)a --(CH2)b --(T)c --B; a is 0 or 1; b is 3 to 14; c is 0 or 1; L and T are independently sulfur, oxygen, CH=CH, C C, or CH2 ; B is H, C1-4 alkyl, ethynyl, trifluoromethyl, isopropenyl, furanyl, thienyl, cyclohexyl or phenyl unsubstituted or monosubstituted by Br, Cl, CF3, C1-4 alkoxy, C1-4 alkyl, methylthio or trifluoromethylthio; R2 and A are independently selected from H, CF3, C1-4 alkyl, C1-4 alkoxy, F, Cl, Br, I, OH, NO2 or NH2 ; or, when R1 and A are H, R2 is (L)a --(CH2)b --(T)c --B wherein a, b, c, L, T and B are as defined above; and M is H, Li, Na, K, NH4 or an organic ammonium cation, and their use in a process for preparing leukotriene antagonists.

Leukotriene antagonists

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, (2008/06/13)

This invention relates to alkanoic acid compounds having phenyl and heteroarylthio substituents which are useful as leukotriene antagonists, pharmaceutical compositions containing such compounds, and methods of treating diseases in which leukotrienes are a factor by administration of an effective amount of the above compounds or compositions.

Leukotriene antagonists

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, (2008/06/13)

This invention relates to alkanoic acid compounds having phenyl and sulfinyl or sulfonyl substituents which are useful as leukotriene antagonists and pharmaceutical compositions containing such compounds. The invention also relates to the use of such compound for treatment of diseases in which leukotrienes are a factor.

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