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CAS

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2,2-diethoxy-ethanimidic acid methyl ester, also known as ethyl 2,2-diethoxyethanimidate, is a chemical compound characterized by its molecular formula C7H15NO3. It is a white solid with a bitter taste and is recognized for its extensive industrial applications.

76742-48-8

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76742-48-8 Usage

Uses

Used in Pesticide Industry:
2,2-diethoxy-ethanimidic acid methyl ester is used as an active ingredient in pesticides for its ability to control and manage various pests, thereby protecting crops and enhancing agricultural productivity.
Used as an Intermediate in Organic Synthesis:
In the chemical industry, 2,2-diethoxy-ethanimidic acid methyl ester serves as a valuable intermediate in the synthesis of a variety of organic compounds, contributing to the development of new materials and products.
Used in Pharmaceutical Industry:
2,2-diethoxy-ethanimidic acid methyl ester is utilized as a building block in the pharmaceutical sector for the production of drugs, playing a crucial role in the creation of medicinal compounds that address various health conditions.
Safety Note:
It is important to handle 2,2-diethoxy-ethanimidic acid methyl ester with care due to its harmful nature if ingested or inhaled, and its potential to cause skin and eye irritation upon contact. Proper safety measures should be implemented during its use in any application.

Check Digit Verification of cas no

The CAS Registry Mumber 76742-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,4 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76742-48:
(7*7)+(6*6)+(5*7)+(4*4)+(3*2)+(2*4)+(1*8)=158
158 % 10 = 8
So 76742-48-8 is a valid CAS Registry Number.

76742-48-8SDS

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 Methyl 2,2-diethoxyethanimidate

1.2 Other means of identification

Product number -
Other names methyl diethoxyacetimidate

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:76742-48-8 SDS

76742-48-8Relevant articles and documents

Steric interference on the redox-conjugated pyrimidine ring rotation of monoand dinuclear copper complexes with (4-Methyl-2-pyrimidinyl)imine ligands

Hattori, Yohei,Nishikawa, Michihiro,Kusamoto, Tetsuro,Kume, Shoko,Nishihara, Hiroshi

, p. 1037 - 1039 (2014)

A mononuclear copper(I) complex with N-[(4-methyl-2- pyrimidinyl)methylene] -p-toluidine (1?BF4) and a dinuclear copper(I) complex with N,N'-bis[(4-methyl-2-pyrimidinyl)- methylene]-p-phenylenediamine (2?(BF4)2) were synth

HETEROCYCLIC COMPOUNDS AS INHIBITORS OF HPK1

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Page/Page column 20; 214, (2021/01/29)

This disclosure relates to heterocyclics as inhibitors of HPK1, in particular relates to a compound of Formula I or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition comprising said compound that useful for treatment of HPK1 mediated diseases and conditions such as cancer. (I)

MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR 2

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Page/Page column 74, (2021/08/06)

The present application provides a compound of Formula: or a pharmaceutically acceptable salt thereof, wherein ring B, L1, ring A, L2, n, R1, R2, R3, R4, and X1 are as described herein. Pharmaceutical compositions comprising the compound, as well as the methods of making and using the compound, are also provided.

MAP4K1 INHIBITORS

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Page/Page column 234; 235, (2021/07/24)

One embodiment of the disclosure is a compound represented by Formula I or a pharmaceutically acceptable salt thereof. The variables in Formula I are defined herein. Compounds of Formula I are selective MAP4K1 inhibitors, which can be used to treat a diseases or disorders in a subject that benefits from control of MAP4K1 activity.

ISOQUINOLINE COMPOUNDS AND USES THEREOF

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Paragraph 0281-0282; 0317, (2020/02/16)

Isoquinoline compounds of formula (I) variations thereof, and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the isoquinoline compounds.

ISOQUINOLINE COMPOUNDS FOR THE TREATMENT OF CANCER

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Paragraph 0294, (2020/05/15)

3-Carbonylaminoisoquinoline compounds of formula (I): variations thereof, and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibiting HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the 3-carbonylaminoisoquinoline compounds.

SMARCA INHIBITORS AND USES THEREOF

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Paragraph 00163-00164, (2020/12/30)

The present invention provides compounds, pharmaceutically acceptable compositions thereof, and methods of using the same for the modulation of one or more SWI/SNF-related matrix associated actin dependent regulator of chromatin subfamily A (SMARCA) and/or polybromo-1 (PB-1) protein via ubiqitination and/or degradation by compounds. The compounds are useful in treatment of cancer.

DIAZANAPHTHALEN-3-YL CARBOXAMIDES AND PREPARATION AND USE THEREOF

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Paragraph 0909-0910, (2019/05/15)

Diazanaphthalene compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of a diazanaphthalene compound or analogs thereof, in the treatment of disorders characterized by the activa

ISOQUINOLINES AS INHIBITORS OF HPK1

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Paragraph 0427, (2018/10/21)

Isoquinoline compounds and their use as inhibitors of HPK1 (hematopoietic kinase 1) are described. The compounds are useful in treating HPK1-dependent disorders and enhancing an immune response. Also described are methods of inhibitng HPK1, methods of treating HPK1-dependent disorders, methods for enhancing an immune response, and methods for preparing the isoquinoline compounds.

METALLO-BETA-LACTAMASE INHIBITORS

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Page/Page column 68; 69, (2017/04/04)

The present invention relates to compounds of formula I that are metallo-β-lactamase inhibitors, the synthesis of such compounds, and the use of such compounds for use with β-lactam antibiotics for overcoming resistance.

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