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2-methyl-2-(methylsulfonyl)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25841-43-4

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25841-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25841-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,4 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25841-43:
(7*2)+(6*5)+(5*8)+(4*4)+(3*1)+(2*4)+(1*3)=114
114 % 10 = 4
So 25841-43-4 is a valid CAS Registry Number.

25841-43-4SDS

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 2-methyl-2-methylsulfonylpropanoic acid

1.2 Other means of identification

Product number -
Other names Propionic acid,2-methyl-2-(methylsulfonyl)

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:25841-43-4 SDS

25841-43-4Relevant academic research and scientific papers

OXADIAZOLE COMPOUNDS

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Paragraph 00519, (2019/12/04)

Provided herein are compounds and pharmaceutical compositions comprising said compounds that are useful for treating cancers. Specific cancers include those that are mediated by YAP/TAZ or those that are modulated by the interaction between YAP/TAZ and TEAD.

Hepatitis C Virus Inhibitors

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Paragraph 2319-2320, (2015/02/25)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

COMBINATIONS OF HEPATITIS C VIRUS INHIBITORS

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Page/Page column 730, (2015/02/02)

The present disclosure is generally directed to antiviral compounds, and more specifically directed to combinations of compounds which can inhibit the function of the NS5A protein encoded by Hepatitis C virus (HCV), compositions comprising such combinations, and methods for inhibiting the function of the NS5A protein.

Compounds which Modulate the CB2 Receptor

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Page/Page column 11, (2008/06/13)

Compounds of formula (I) are disclosed. Compounds according to the invention bind to and are agonists, antagonists or inverse agonists of the CB2 receptor, and are useful for treating inflammation. Those compounds which are agonists are additionally usefu

Pyridylthio-acylanilide herbicides

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, (2008/06/13)

Novel herbicidally active pyridylthio-acylanilides of the formula STR1 in which R1, R2 and R3, independently of one another, represent hydrogen, halogen, cyano or trifluoromethyl or alkyl, alkoxy and alkylthio having 1 to 4 carbon atoms in each case, R4 represents halogen, methyl or methoxy, n represents a number 0, 1 or 2, z represents the group (Ia) STR2 or the group (Ib) STR3 where X represents oxygen, sulphur, an N--R10 or N--O--R11 group, or X and Rg tpgether represent the STR4 radical, and the other radicals can have various meanings. Intermediates of the formulae STR5 are also new.

Catalyse de l'oxydation par l'acid peracetique de sulfures organiques, contenant des fonctions fragiles, en sulfoxydes et sulfones correspondants

Rouchard, Jean,Moons, Chantal,Meyer, Joseph

, p. 441 - 443 (2007/10/02)

Organic sulfur compounds which contained supplementary susceptible functions (oxime, nitrile, acid, alcohol, oximecarbamate) were separately oxidised into the corresponding sulfoxides and sulfones with an anhydrous peracetic acid solution.Molybdenyl acetonylacetonate catalysed the oxidation toward the best conversions of the peracid, and the best selectivities for the sulfoxides and sulfones.

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