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7693-49-4

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7693-49-4 Usage

Physical state

Highly reactive and volatile compound

Usage

Organic synthesis, reagent in chemical reactions

Notable functional group

Carbonyl chloride

Importance

Preparation of various organic compounds

Industries

Pharmaceutical and agrochemical

Safety

Handle with care, follow proper safety procedures

Check Digit Verification of cas no

The CAS Registry Mumber 7693-49-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,9 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7693-49:
(6*7)+(5*6)+(4*9)+(3*3)+(2*4)+(1*9)=134
134 % 10 = 4
So 7693-49-4 is a valid CAS Registry Number.

7693-49-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,6-di(propan-2-yl)phenyl] carbonochloridate

1.2 Other means of identification

Product number -
Other names Chlorameisensaeure-<2,6-diisopropyl-phenylester>

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:7693-49-4 SDS

7693-49-4Relevant articles and documents

Cobalt-Nitrenoid Insertion-Mediated Amidative Carbon Rearrangement via Alkyl-Walking on Arenes

Lee, Jeonghyo,Kang, Bora,Kim, Dongwook,Lee, Jia,Chang, Sukbok

supporting information, p. 18406 - 18412 (2021/11/16)

We herein disclose the Cp*Co(III)(LX)-catalyzed amidative alkyl migration using 2,6-disubstituted phenyl azidoformates. Upon the cobalt-nitrenoid insertion toward the substituted ortho carbon, an arenium cationic species bearing a quaternary carbon is generated, and a subsequent alkyl migration process is suggested to occur through an unforeseen alkyl-walking mechanism. A quinolinol ligand of the cobalt catalyst system is proposed to facilitate the final product-releasing rearomatization process by serving as an internal base. This new mechanistic mode enabled both [1,2]- and [1,4]-alkyl rearrangements to allow the structural variation of N-heterocyclic compounds.

Phosphoric acid derivative as well as preparation method and application

-

Paragraph 0118; 0122-0126, (2019/03/24)

The invention relates to a compound shown in a general formula (I), a stereoisomer or pharmaceutically acceptable salt thereof as well as an application in medicines. The structure of the compound inthe general formula (I) is shown in the description, and

SERINE AMINO ACID DERIVED PRODRUGS OF PROPOFOL, COMPOSITIONS, USES AND CRYSTALLINE FORMS THEREOF

-

Page/Page column 23; 47, (2008/06/13)

The present invention provides a prodrug of propofol and crystalline forms thereof, methods of making the propofol prodrug and crystalline forms thereof, pharmaceutical compositions of the propofol prodrug and crystalline forms thereof, methods of using t

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