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78357-63-8

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78357-63-8 Usage

Description

(3,5-dimethylphenoxy)acetyl chloride is a chemical compound with the molecular formula C10H11ClO2. It is an acetylating agent commonly used in organic synthesis and pharmaceutical research. (3,5-dimethylphenoxy)acetyl chloride is a clear and colorless liquid with a pungent odor. Due to its high reactivity, it must be handled with care to avoid irritation to the skin, eyes, and respiratory system.

Uses

Used in Pharmaceutical Research:
(3,5-dimethylphenoxy)acetyl chloride is used as an acetylating agent for the synthesis of pharmaceuticals. It aids in the development of new drugs by facilitating the acetylation of various organic compounds, which can enhance their properties or create new therapeutic agents.
Used in Agrochemical Synthesis:
In the agrochemical industry, (3,5-dimethylphenoxy)acetyl chloride is used as a key intermediate in the synthesis of various agrochemicals. Its acetylating properties allow for the creation of new compounds that can be used in pest control, crop protection, and other agricultural applications.
Used in Organic Synthesis:
(3,5-dimethylphenoxy)acetyl chloride is utilized as a reagent in organic synthesis for the production of a wide range of organic compounds. Its versatility in acetylation reactions makes it a valuable tool in the synthesis of various organic molecules for research and commercial purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 78357-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,5 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 78357-63:
(7*7)+(6*8)+(5*3)+(4*5)+(3*7)+(2*6)+(1*3)=168
168 % 10 = 8
So 78357-63-8 is a valid CAS Registry Number.

78357-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,5-dimethylphenoxy)acetyl chloride

1.2 Other means of identification

Product number -
Other names Acetyl chloride,(3,5-dimethylphenoxy)

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:78357-63-8 SDS

78357-63-8Relevant articles and documents

INHIBITORS TO TARGET HIV-1 NEF-CD80/CD86 INTERACTIONS FOR THERAPEUTIC INTERVENTION

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Paragraph 000169, (2020/03/05)

The compounds of Formula I, II, and III along with their stereoisomers, pharmaceutically acceptable salts, polymorphs, solvates and hydrates thereof are described in the present disclosure. The said compounds restore immune activation in case of infections or a disease associated with an HIV infection in a subject in need thereof.

Photoassisted Synthesis of Complex Molecular Architectures: Dearomatization of Benzenoid Arenes with Aza-o-xylylenes via an Unprecedented [2+4] Reaction Topology

Kuznetsov, Dmitry M.,Mukhina, Olga A.,Kutateladze, Andrei G.

supporting information, p. 6988 - 6991 (2016/06/13)

A new method was developed for the photoinduced dearomatization of arenes through an intramolecular cycloaddition with aza-o-xylylenes generated by excited-state intramolecular proton transfer (ESIPT) in the readily available photoprecursors. The [2+4] topology of this cycloaddition is unprecedented for photo-dearomatizations of benzenoid aromatic carbocycles. It provides rapid access to novel heterocycles, cyclohexadieno-oxazolidino-quinolinols, as valuable synthons for a broad range of post-photochemical transformations. I'm so excited: Photoinduced dearomatization of arenes was achieved through intramolecular cycloaddition with aza-o-xylylenes generated by excited-state intramolecular proton transfer in the readily available photoprecursors. The [2+4] topology of this cycloaddition is unprecedented for photo-dearomatizations of benzenoid aromatic carbocycles and produces the novel heterocycles cyclohexadieno-oxazolidino-quinolinols.

1-arylsulfonyl-2-(Pyridylmethylsulfinyl) benzimidazoles as new proton pump inhibitor prodrugs

Shin, Jai Moo,Sachs, George,Cho, Young-Moon,Garst, Michael

experimental part, p. 5247 - 5280 (2010/03/30)

New arylsulfonyl proton pump inhibitor (PPI) prodrug forms were synthesized. These prodrugs provided longer residence time of an effective PPI plasma concentration, resulting in better gastric acid inhibition.

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