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70639-94-0

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70639-94-0 Usage

General Description

1-cyclopentyl-3-(triMethylsilyl)prop-2-yn-1-one is a chemical compound with the molecular formula C10H18OSi. It is a propargyl ketone derivative that contains a cyclopentyl group and a trimethylsilyl group. 1-cyclopentyl-3-(triMethylsilyl)prop-2-yn-1-one is commonly used in organic synthesis as a reagent for the preparation of various organic compounds. It is also used as a building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, 1-cyclopentyl-3-(triMethylsilyl)prop-2-yn-1-one exhibits unique chemical properties that make it a valuable tool for research and development in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 70639-94-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,6,3 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 70639-94:
(7*7)+(6*0)+(5*6)+(4*3)+(3*9)+(2*9)+(1*4)=140
140 % 10 = 0
So 70639-94-0 is a valid CAS Registry Number.

70639-94-0SDS

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 3-cyclopentyl-1-trimethylsilyl-1-propyn-3-one

1.2 Other means of identification

Product number -
Other names cyclopentyl trimethylsilylethynyl ketone

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:70639-94-0 SDS

70639-94-0Relevant articles and documents

Gold-Catalyzed Dehydrogenative Cycloisomerization of 1,4-Enyne Esters to 3,5-Disubstituted Phenol Derivatives

Chen, Cuili,Chen, Xianxiao,Zhang, Xiaoxiang,Wang, Shifa,Rao, Weidong,Chan, Philip Wai Hong

, p. 4359 - 4368 (2017/12/26)

A method to prepare synthetically important 3,5-disubstituted phenol derivatives that relies on the sequential gold(I)-catalyzed dehydrogenative cycloisomerization of 1,4-enyne esters in the presence of 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) or N-fluorobenzenesulfonimide (NFSI) is described. The synthetic versatility of the methodology was exemplified by a gram-scale reaction of one example, the ease to realize subsequent functional transformations of an adduct, and the application of the method to the synthesis of the bioactive molecule LUF5771. (Figure presented.).

INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME

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Page 113, (2008/06/13)

The invention relates to compounds of the formula (I) and to pharmaceutically acceptable salts, solvates, prodrugs and metabolites thereof, wherein W, Z, R1and R2, are as defined herein. The invention also relates to methods of treating Hepatitis C virus in mammals by administering the compounds of formula (I), and to pharmaceutical compositions for treating such disorders, which contain the compounds of formula (I). The invention also relates to methods of preparing the compounds of formula (I).

INHIBITORS OF HEPATITIS C VIRUS RNA-DEPENDENT RNA POLYMERASE, AND COMPOSITIONS AND TREATMENTS USING THE SAME

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Page/Page column 57, (2010/02/07)

Compounds of formula (I) are hepatitis C virus (HCV) RNA-dependent RNA polymerase (RdRp) inhibitors, and are useful in therapeutic and prophylactic treatment of persons infected with hepatitis C virus.

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