Welcome to LookChem.com Sign In|Join Free
  • or
2-Chloro-N-(2-methoxyethyl)acetamide is a unique organic compound with the molecular formula C5H10ClNO2. It is an amide derivative, where one or more hydrogen atoms are replaced by an alkyl group. 2-CHLORO-N-(2-METHOXYETHYL)ACETAMIDE is characterized by the presence of a chlorine atom attached to one of the carbons and a methoxyethyl side chain. Due to its reactivity, especially because of the chlorine atom, it is essential to handle this chemical with care.

10263-66-8

Post Buying Request

10263-66-8 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

10263-66-8 Usage

Uses

Used in Organic Synthesis:
2-Chloro-N-(2-methoxyethyl)acetamide is used as an intermediate in various organic synthesis processes. Its unique structure allows it to be a valuable component in the creation of more complex molecules, which can be utilized in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Chloro-N-(2-methoxyethyl)acetamide is used as a building block for the development of new drugs. Its specific chemical properties make it a potential candidate for medicinal applications, contributing to the synthesis of therapeutic agents.
Used in Agricultural Applications:
2-Chloro-N-(2-methoxyethyl)acetamide is also used in the agricultural sector, particularly in the synthesis of agrochemicals. Its role in creating new compounds can lead to the development of more effective pesticides or other agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 10263-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10263-66:
(7*1)+(6*0)+(5*2)+(4*6)+(3*3)+(2*6)+(1*6)=68
68 % 10 = 8
So 10263-66-8 is a valid CAS Registry Number.

10263-66-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-N-(2-METHOXYETHYL)ACETAMIDE

1.2 Other means of identification

Product number -
Other names N-(2-methoxyethyl)-chloroacetamide

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:10263-66-8 SDS

10263-66-8Relevant academic research and scientific papers

Inhibition of tumor cell growth by a specific 6-phosphofructo-2-kinase inhibitor, N-bromoacetylethanolamine phosphate, and its analogues.

Hirata,Watanabe,Miura,Ijichi,Fukasawa,Sakakibara

, p. 2047 - 2052 (2000)

The high rate of glycolysis despite the presence of oxygen and mitochondria in tumor cells implies an important role for this process in cell division. The rate of glycolysis is assumed to be dependent on the cellular concentration of fructose 2,6-bisphosphate, the concentration of which in turn depends on a bifunctional enzyme and the ratio of this enzyme's 6-phosphofructo-2-kinase versus its fructose 2,6-bisphosphatase activities. To prove the hypothesis that inhibition of glycolysis in tumor cells by 6-phosphofructo-2-kinase inhibitors would cause inhibition of tumor cell proliferation, ten N-bromoacetylethanolamine phosphate analogues were designed, synthesized, and tested. They were screened for their activities against various human tumor cell lines to study the effects of inhibition of glycolysis on cell proliferation. The relationship between the structure of these compounds and their inhibitory activity on cell proliferation was also discussed. It was found that the activity of N-(2-methoxyethyl)-bromoacetamide, N-(2-ethoxyethyl)-bromoacetamide, and N-(3-methoxypropyl)-bromoacetamide was comparable to that of the positive control AraC. These three inhibitors showed in vivo anticancer effects in P388 transplant BDF1 mice.

Phosphatase Binding Compounds and Methods of Using Same

-

Paragraph 2; 232; 236-237, (2020/07/25)

The present invention provides bifunctional compounds that efficiently dephosphorylate certain phospho-activated target proteins. Such target proteins can be any protein involved in the pathway of a disease or disorder, such as but not limited to cancer, neurodegeneration, metabolic disease, diabetes, insulin resistance, and so forth.

PRO-SURVIVAL COMPOUNDS

-

Page/Page column 34, (2016/07/05)

Disclosed herein are a class of compounds useful in cell culture, in particular, the in vitro culture of stem cells. The compounds have been found to promote the survival and/or maintenance of stem cells in (or during) culture and/or throughout passage.

Selective β3-adrenergic agonists of brown adipose tissue and thermogenesis. 2. [4-[2-[(2-Hydroxy-3- phenoxypropyl)amino]ethoxy]phenoxy]acetamides

Howe,Rao,Holloway,Stribling

, p. 1759 - 1764 (2007/10/02)

The ester methyl [4-[2-[(2-hydroxy-3- phenoxypropyl)amino]ethoxy]phenoxy]acetate (1) (R1 = OMe) had previously been identified as the most interesting member of a series of selective β3- adrenergic agonists of brown adipose tissue an

Composition for magnetic resonance imaging

-

, (2008/06/13)

Methods and compositions for enhancing magnetic resonance imaging in at least a portion of a warm-blooded animal.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 10263-66-8