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1,3,5-Pentanetricarboxylic acid, 3-[[(4-chlorophenyl)methylene]amino]-, trimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113845-87-7

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113845-87-7 Usage

Explanation

The compound's full name, which describes its structure and functional groups.

Explanation

A shorter, more commonly used name for the compound.

Explanation

It is a substance formed from two or more elements chemically bonded together.

Explanation

The compound is derived from pentanetricarboxylic acid, which means it has a similar structure with additional functional groups.

Explanation

The compound is used as an intermediate in the synthesis of various products, including pharmaceuticals, agrochemicals, and other specialty chemicals. It is also utilized in research and development applications.

Explanation

The compound's structure consists of a pentanetricarboxylic acid core, with a trimethyl ester group on one end and a 4-chlorophenylmethyleneamino group on the other, making it a versatile building block for organic synthesis.

Explanation

The compound contains various functional groups, including an ester (trimethyl ester), an amide (methyleneamino), an aromatic ring (4-chlorophenyl), and a halogen (chlorine).

Explanation

The molecular formula represents the number of atoms of each element in a molecule of the compound (16 carbon, 16 hydrogen, 1 chlorine, 1 nitrogen, and 6 oxygen atoms).

Explanation

The molecular weight is the sum of the atomic weights of all the atoms in the molecule.

Explanation

The compound is likely to dissolve in organic solvents, such as ethanol, methanol, or acetone, due to its nonpolar nature.

Type

Chemical compound

Derivative

Pentanetricarboxylic acid

Applications

Pharmaceutical synthesis, agrochemicals, specialty chemicals, research and development

Structure

Central pentanetricarboxylic acid core, trimethyl ester group, 4-chlorophenylmethyleneamino group

Functional Groups

Ester, amide, aromatic ring, halogen

Molecular Weight

Approximately 355.76 g/mol

Solubility

Soluble in organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 113845-87-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,4 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113845-87:
(8*1)+(7*1)+(6*3)+(5*8)+(4*4)+(3*5)+(2*8)+(1*7)=127
127 % 10 = 7
So 113845-87-7 is a valid CAS Registry Number.

113845-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-{[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-amino}-4-methoxycarbonyl-heptanedioic acid dimethyl ester

1.2 Other means of identification

Product number -
Other names -

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:113845-87-7 SDS

113845-87-7Downstream Products

113845-87-7Relevant academic research and scientific papers

A CONVENIENT CATALYTIC SYSTEM OF POTASSIUM CARBONATE AND ALKANOL: THE MICHAEL ADDITION AND CARBONYL ADDITION REACTIONS OF IMINE COMPOUNDS

Changyou, Zhou,Daimo, Chen,Yaozhong, Jiang

, p. 1377 - 1382 (2007/10/02)

The nucleophilic addition of imine compounds to dipolarophiles can be conveniently performed in protic alkanol solvents using solid K2CO3 as a base.This method may be adapted on the large scale preparation of glutamine and serine derivatives.

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