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Allyl 4-chloro-2-(allyloxy)benzoate is a chemical compound with the molecular formula C12H13ClO3. It is an organic ester derived from 4-chloro-2-hydroxybenzoic acid, where the hydroxyl group is replaced by an allyl ether group. allyl 4-chloro-2-(allyloxy)benzoate is characterized by its chlorine atom at the para position of the benzene ring and two allyl groups attached to the benzene ring and the carboxylic acid group, respectively. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can participate in various chemical reactions, such as polymerization and condensation, making it a versatile building block in organic chemistry.

93856-97-4

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93856-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93856-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,5 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93856-97:
(7*9)+(6*3)+(5*8)+(4*5)+(3*6)+(2*9)+(1*7)=184
184 % 10 = 4
So 93856-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H13ClO3/c1-3-7-16-12-9-10(14)5-6-11(12)13(15)17-8-4-2/h3-6,9H,1-2,7-8H2

93856-97-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl 4-chloro-2-prop-2-enoxybenzoate

1.2 Other means of identification

Product number -
Other names Allyl 4-chloro-2-(allyloxy)benzoate

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

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More Details:93856-97-4 SDS

93856-97-4Relevant academic research and scientific papers

The Synthesis of 5-Amino-dihydrobenzo[b]oxepines and 5-Amino-dihydrobenzo[b]azepines via Ichikawa Rearrangement and Ring-Closing Metathesis

Chwastek, Monika,Pieczykolan, Micha?,Stecko, Sebastian

, p. 9046 - 9074 (2016/10/17)

The combination of Ichikawa's rearrangement and a ring-closing metathesis reaction of allyl carbamates is presented as a method for the preparation of 5-amino-substituted 2,5-dihydro-benzo[b]oxepines, 2,5-dihydro-benzo[b]azepines, and 2,5-dihydro-benzo[b]thiepins. It was demonstrated that the use of nonracemic allyl carbamates enables the synthesis of enantioenriched benzo-fused seven-membered heterocycles. Finally, it was shown that further functionalization of the obtained structures allows access to pharmacologically active 5-amino-substituted 2,3,4,5-tetrahydro-1-benzo[b]oxepine scaffolds.

General route for the preparation of diverse 17-membered macrocycles based on RCM and examination of the E/Z selectivity

Heckrodt, Thilo J.,Singh, Rajinder

experimental part, p. 2854 - 2865 (2012/07/16)

(Chemical Equation Presented) A convergent, general synthetic route to 17-membered macrocycles was developed to support biological evaluation and structure-activity relationship (SAR) studies during phenotypic screening for immunology targets. A series of amide coupling reactions led to a ring-closing metathesis (RCM) precursor that was cyclized using Grubbs' catalysts. It was found that the reaction formed the macrocyclic products in a 3:1 ratio of E/Z isomers. Moreover, it was shown that a number of similarly substituted RCM precursors undergo cyclization to produce the geometric E/Z isomers in roughly the same 3:1 ratio. The remarkable independence of the E/Z outcome from the substitution pattern of the RCM precursor makes this synthetic approach generally applicable. Separation of the E/Z isomers was achieved by preparative high-performance liquid chromatography and allowed biological profiling of the geometric isomers. Reactive groups in the macrocycle were utilized for late-stage modifications in the fashion of diversity-orientated synthesis (DOS), yielding analogs for SAR studies. Copyright Rigel Pharmaceuticals, Inc.

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