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2-CHLORO-N-(5-CHLORO-2-METHOXYPHENYL)ACETAMIDE, with the chemical formula C9H8Cl2N2O2, is a chloroacetamide and an anisole derivative belonging to the acetamide family of organic compounds. It is a significant intermediate in organic synthesis and pharmaceutical research due to its unique structure, which includes a chloroacetamide group, a chlorobenzene group, and an anisole group.
Used in Pharmaceutical Industry:
2-CHLORO-N-(5-CHLORO-2-METHOXYPHENYL)ACETAMIDE is used as a building block for the manufacturing of pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of various other compounds, making it valuable in the development of new drugs and medications.
Used in Organic Synthesis:
2-CHLORO-N-(5-CHLORO-2-METHOXYPHENYL)ACETAMIDE is used as an important intermediate in organic synthesis. Its versatile structure enables it to be incorporated into a wide range of chemical reactions, facilitating the creation of new compounds and materials for various applications.

35588-41-1

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35588-41-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35588-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,8 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35588-41:
(7*3)+(6*5)+(5*5)+(4*8)+(3*8)+(2*4)+(1*1)=141
141 % 10 = 1
So 35588-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl2NO2/c1-14-8-3-2-6(11)4-7(8)12-9(13)5-10/h2-4H,5H2,1H3,(H,12,13)

35588-41-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-N-(5-chloro-2-methoxyphenyl)acetamide

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:35588-41-1 SDS

35588-41-1Relevant academic research and scientific papers

Discovery of a Potent Botulinum Neurotoxin A Inhibitor ZM299 with Effective Protections in Botulism Mice

Gao, Jie,He, Zhili,Hong, Zhanying,Li, Tao,Luo, Deyan,Miao, Zhenyuan,Ning, Nianzhi,Wang, Hui,Wang, Jianxin,Wu, Yuelin,Xv, Xiguo,Zhang, Wannian,Zhang, Yanming,Zhuang, Chunlin

, p. 357 - 364 (2021/12/24)

Botulinum neurotoxins serotype A (BoNT/A) is the deadliest toxins known to humans and the "Category A" agent for bioterrorism. Over the past 20 years, significant efforts have been put forth to develop effective inhibitors of BoNT/A. Unfortunately, few id

Nicotinic acid or isonicotinic acid compound and application thereof

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Paragraph 0066, (2017/08/25)

The invention discloses a nicotinic acid or isonicotinic acid compound and application thereof. The compound provided by the invention is a compound as shown in formula I or the pharmaceutically acceptable salt, ester and solvate thereof. Proved by pharmacodynamic test, the sulfydryl nicotinic acid type compound provided by the invention can inhibit the activity of botulinum toxin endoprotease in vitro, and has an obvious protection effect on mice suffering from botulinum toxin poisoning. On the basis, the compound provided by the invention can be used for preparing and/or treating drugs with botulinum toxin exposure and/or poisoning.

MERCAPTONICOTINIC ACID COMPOUND AND PREPARATION METHOD AND USE THEREOF

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Paragraph 0074-0079, (2016/04/19)

The present invention discloses a class of mercaptonicotinic acid compound and preparation method and use thereof; the general structural formula of the compound is as shown in Formula I. Experiment demonstrates that the mercaptonicotinic acid compound co

BENZENESULFONAMIDE COMPOUNDS AND THEIR USE AS BLOCKERS OF CALCIUM CHANNELS

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Page/Page column 179-180, (2010/11/28)

The invention relates to piperidinyl and hexahydroazepinyl compounds of Formula (I): and pharmaceutically acceptable salts, prodrugs, or solvates thereof, wherein R1-R3, Z and q are defined as set forth in the specification. The inve

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