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Acetic acid, (1-cyclohexen-1-yloxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64825-54-3

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64825-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64825-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,8,2 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64825-54:
(7*6)+(6*4)+(5*8)+(4*2)+(3*5)+(2*5)+(1*4)=143
143 % 10 = 3
So 64825-54-3 is a valid CAS Registry Number.

64825-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(cyclohexen-1-yloxy)acetate

1.2 Other means of identification

Product number -
Other names cyclohex-1-enyloxy-acetic acid ethyl ester

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:64825-54-3 SDS

64825-54-3Relevant academic research and scientific papers

ACETAL-BASED CLEAVABLE LINKERS

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Paragraph 0144-0145, (2020/12/29)

The current invention concerns compounds, such as antibody-conjugates, with an enhanced selectivity of payload release inside a tumour or in the tumour microenvironment versus payload release in circulation or in healthy cells. The enhanced selectivity is

REGIO- AND DIASTEREOSELECTIVITY OF ENOL ETHER FORMATION BY 1,4-SIGMATROPIC SHIFTS OF HYDROGEN IN CARBONYL YLIDES

Lottes, Andrew C.,Landgrebe, John A.,Larsen, Kristin

, p. 4089 - 4092 (2007/10/02)

Treatment of aliphatic ketones with ethyl diazoacetate in the presence of a catalyst results in the regio- and (where appropriate) diastereoselective formation of enol ethers which arise by an intramolecular 1,4-hydrogen shift from an intermediate carbony

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