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83935-54-0

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83935-54-0 Usage

Description

DI-METHYL-4-NITRO-4-[2-(METHOXYCARBONYL)ETHYL]HEPTANEDIOATE is a complex organic chemical compound characterized by the presence of di-methyl, nitro, and methoxycarbonyl groups attached to a heptanedioate chain. DI-METHYL-4-NITRO-4-[2-(METHOXYCARBONYL)ETHYL]HEPTANEDIOATE is known for its unique chemical properties and is utilized as a versatile building block in the synthesis of a variety of organic molecules and pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
DI-METHYL-4-NITRO-4-[2-(METHOXYCARBONYL)ETHYL]HEPTANEDIOATE serves as a chemical intermediate in the pharmaceutical industry, playing a crucial role in the synthesis of various organic molecules and drugs. Its unique structure allows for the development of new therapeutic agents with potential applications in treating a range of medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, DI-METHYL-4-NITRO-4-[2-(METHOXYCARBONYL)ETHYL]HEPTANEDIOATE is utilized for the production of pesticides, herbicides, and insecticides. Its chemical properties make it a valuable component in the development of effective and targeted agricultural chemicals that can protect crops and enhance agricultural productivity.
Used in Research and Development:
DI-METHYL-4-NITRO-4-[2-(METHOXYCARBONYL)ETHYL]HEPTANEDIOATE is also employed in research and development laboratories. Its unique chemical properties make it an interesting subject for scientific exploration, potentially leading to the discovery of new applications and advancements in various fields, including materials science, chemical engineering, and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 83935-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,3 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83935-54:
(7*8)+(6*3)+(5*9)+(4*3)+(3*5)+(2*5)+(1*4)=160
160 % 10 = 0
So 83935-54-0 is a valid CAS Registry Number.

83935-54-0SDS

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 4-(3-methoxy-3-oxopropyl)-4-nitroheptanedioate

1.2 Other means of identification

Product number -
Other names 4-(2-methoxycarbonylethyl)-4-nitroheptanedioic acid 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:83935-54-0 SDS

83935-54-0Relevant articles and documents

ARGININE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

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Paragraph 00359, (2016/04/20)

Described herein are compounds of Formula (S-I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds described herein are useful for inhibiting arginine methyltransferase activity. Methods of using the compounds for treating arginine methyltransferase-mediated disorders are also described.

Stereocontrolled total synthesis of (±)-FR901483

Ieda, Shigeru,Asoh, Yusuke,Fujimoto, Teppei,Kitaoka, Haruka,Kan, Toshiyuki,Fukuyama, Tohru

experimental part, p. 721 - 738 (2009/12/26)

The total synthesis of potent immunosuppressant FR901483 (1) is reported. The remarkable feature of our convergent synthesis is the p-methoxybenzyl and methylamino groups are stereoselectively incorporated within the tri-cyclic core skeleton. The skeleton

Phase-transfer-catalysed Preparation of N-Alkylated Trihydroxamic Acids

Hoffmann, Pascal,Doucet, Jean-Baptiste,Li, Wenhao,Vergnes, Laurent,Labidalle, Serge

, p. 218 - 219 (2007/10/03)

We describe a synthetic route involving phase transfer catalysis leading to a series of tripodal N-alkylated hydroxamic acids as models of desferrioxamine; iron(III) exchange reactions between their iron complexes and EDTA were investigated.

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