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61771-75-3

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61771-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61771-75-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,7,7 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61771-75:
(7*6)+(6*1)+(5*7)+(4*7)+(3*1)+(2*7)+(1*5)=133
133 % 10 = 3
So 61771-75-3 is a valid CAS Registry Number.

61771-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-1-prop-2-enylcyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1-allyl-2-oxo-cyclohexanecarboxylic 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:61771-75-3 SDS

61771-75-3Relevant articles and documents

Synthesis of α-hydroxy and α-oxospiranes through ruthenium(II)-catalyzed ring-closing metathesis

Aburel,Romming,Ma,Undheim

, p. 1458 - 1472 (2001)

Efficient methodology for the construction of functionalized spiranes using Ru(II)-catalyzed ring-closing metathesis reactions is described. The substrates were appropriately substituted five-, six- and seven-membered cycloalkanes which were spiroannulate

INHIBITORS OF HISTONE DEACETYLASE USEFUL FOR THE TREATMENT OR PREVENTION OF HIV INFECTION

-

Page/Page column 34; 35, (2020/02/23)

The present invention relates to Compounds of Formula (I): Formula (I) and pharmaceutically acceptable salts or prodrug thereof, wherein R1, R2, R3, Ra, Rb, A and B are as defined herein. The present invention also relates to compositions comprising at least one compound of Formula (I), and methods of using the compounds of Formula (I) for treating or preventing HIV infection in a subject.

Catalytic C?C Bond Formation Using a Simple Nickel Precatalyst System: Base- and Activator-Free Direct C-Allylation by Alcohols and Amines

Sweeney, Joseph B.,Ball, Anthony K.,Smith, Luke J.

supporting information, p. 7354 - 7357 (2018/05/03)

A “totally catalytic” nickel(0)-mediated method for base-free direct alkylation of allyl alcohols and allyl amines is reported. The reaction is selective for monoallylation, uses an inexpensive NiII precatalyst system, and requires no activating reagents to be present.

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