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Propanedioic acid, (1-methylethoxy)-, dimethyl ester, also known as dimethyl 1-methoxypropanedioate, is a chemical compound with the molecular formula C7H12O5. It is an organic ester derived from propionic acid, featuring a 1-methylethoxy group attached to the propanoic acid backbone. Propanedioic acid, (1-methylethoxy)-, dimethyl ester is characterized by its ester functional groups, which contribute to its reactivity and potential applications in various chemical processes. It is a colorless liquid with a molecular weight of 176.17 g/mol. Due to its ester structure, it is soluble in organic solvents and has a relatively low boiling point, making it suitable for use in chemical synthesis and as a solvent in certain industrial applications.

5257-96-5

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5257-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5257-96-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5257-96:
(6*5)+(5*2)+(4*5)+(3*7)+(2*9)+(1*6)=105
105 % 10 = 5
So 5257-96-5 is a valid CAS Registry Number.

5257-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 2-propan-2-yloxypropanedioate

1.2 Other means of identification

Product number -
Other names Propanedioic acid,(1-methylethoxy)-,dimethyl 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:5257-96-5 SDS

5257-96-5Downstream Products

5257-96-5Relevant academic research and scientific papers

CHEMICAL COMPOUNDS AS INHIBITORS OF INTERLEUKIN-1 ACTIVITY

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Paragraph 00787; 00789; 00790, (2018/08/12)

The present disclosure relates to novel sulfonylurea and sulfonyl thiourea compounds and related compounds and their use in treating a disease or condition responsive to modulation of cytokines such as IL-1β and IL-18, modulation of NLRP3 or inhibition of the activation of NLRP3 or related components of the inflammatory process.

Rhodium-carbenoid mediated O-H insertion reactions. O-H insertion vs. H-abstraction and effect of catalyst

Cox, Geoffrey G.,Miller, David J.,Moody, Christopher J.,Sie, Eric-Robert H. B.,Kulagowski, Janusz J.

, p. 3195 - 3212 (2007/10/02)

The synthesis and rhodium mediated O-H insertion reactions of a wide range of diazo compounds are described. The rate at which the diazo compounds decompose in the presence of 2-propanol and the rhodium catalyst is strongly dependent on the electron withdrawing group(s) attached to the diazo carbon, with diazophosphonates being the least reactive. Insertion into the O-H bond of methanol, t-butanol and phenols was also investigated, as well as the effect of catalyst. In some cases 'reduction' of the diazo group to the corresponding CH2 group competes with O-H insertion, although this is highly catalyst and substrate dependent. Of the catalysts used, rhodium(II) trifluoroacetamide is the most effective for O-H insertion reactions.

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