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[(4-methoxyphenyl)methyl] hydrogen [4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]malonate is a complex organic compound characterized by the presence of a methoxyphenylmethyl group, a tetrahydro-2H-pyran-2-yl group, and a malonate group. Its unique structure and reactivity endow it with potential applications across various fields, making it a significant target for chemical research and development.

70653-29-1

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70653-29-1 Usage

Uses

Used in Pharmaceutical Industry:
[(4-methoxyphenyl)methyl] hydrogen [4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]malonate is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique functional groups allow for the development of new chemical entities with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-methoxyphenyl)methyl] hydrogen [4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]malonate is used as a precursor for the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features enable the creation of novel compounds with improved efficacy and selectivity.
Used in Materials Science:
[(4-methoxyphenyl)methyl] hydrogen [4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]malonate is utilized in materials science for the development of new materials with specific properties. Its functional groups can be exploited to create polymers, coatings, and other materials with tailored characteristics for various applications.
Used in Chemical Research and Development:
As a complex organic compound with multiple functional groups, [(4-methoxyphenyl)methyl] hydrogen [4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]malonate serves as an important target for chemical research and development. Its synthesis and properties are studied to gain insights into new reaction mechanisms, catalysis, and the development of innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 70653-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70653-29:
(7*7)+(6*0)+(5*6)+(4*5)+(3*3)+(2*2)+(1*9)=121
121 % 10 = 1
So 70653-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C22H24O7/c1-26-17-9-5-15(6-10-17)14-28-22(25)20(21(23)24)16-7-11-18(12-8-16)29-19-4-2-3-13-27-19/h5-12,19-20H,2-4,13-14H2,1H3,(H,23,24)

70653-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-methoxyphenyl)methoxy]-2-[4-(oxan-2-yloxy)phenyl]-3-oxopropanoic acid

1.2 Other means of identification

Product number -
Other names 2-[4-(2-tetrahydropyranyloxy)phenyl] malonic acid 4'-methoxybenzyl mono-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:70653-29-1 SDS

70653-29-1Upstream product

70653-29-1Downstream Products

70653-29-1Relevant academic research and scientific papers

Process for the production of phenylmalonic acid mono-esters

-

, (2008/06/13)

Sodium salts of phenylmalonic acid mono-esters are produced by reacting a phenylacetic acid ester with carbon dioxide in the presence of a sodium substituted compound, which is prepared by substituting a sodium atom for a hydrogen atom of an organic compound selected from a group consisting of acetylene, cumene, triphenylmethane, methyl-methylthiomethyl-sulfoxide and dimethyl-sulfoxide, at a temperature in a range of -20° C. to -40° C.

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