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138616-36-1

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  • 1-Cyclopentene-1-carboxylic acid, 2-(phenylethynyl)-, ethyl ester

    Cas No: 138616-36-1

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138616-36-1 Usage

Structure

Ethyl ester derivative of 2-(phenylethynyl)cyclopent-1-ene-1-carboxylic acid
A specific arrangement of atoms, with an ethyl group (C2H5) attached to a cyclopent-1-ene-1-carboxylic acid structure through an ester bond.

Usage

Pharmaceutical industry, synthesis of pharmaceuticals and agrochemicals, production of fine chemicals
The compound serves as a starting material or building block in the creation of various drugs, pesticides, and other high-value chemical products.

Role

Important intermediate in the production of numerous pharmaceutical products
The compound is known for its ability to act as a building block in the synthesis of various biologically active compounds, making it a crucial component in the development of many medications.

Check Digit Verification of cas no

The CAS Registry Mumber 138616-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,6,1 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 138616-36:
(8*1)+(7*3)+(6*8)+(5*6)+(4*1)+(3*6)+(2*3)+(1*6)=141
141 % 10 = 1
So 138616-36-1 is a valid CAS Registry Number.

138616-36-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-phenylethynyl)cyclopentene-1-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2-(phenylethynyl)cyclopentanecarboxylate

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:138616-36-1 SDS

138616-36-1Relevant articles and documents

Synthesis of isocoumarins and α-pyrones via electrophilic cyclization

Yao, Tuanli,Larock, Richard C.

, p. 5936 - 5942 (2007/10/03)

A variety of substituted isocoumarins and α-pyrones are readily prepared in excellent yields under very mild reaction conditions by the reaction of o-(1-alkynyl)benzoates and (Z)-2-alken-4-ynoates with ICl, I2, PhSeCl, p-O2NC6/

Photoinduced DNA cleavage by designed molecules with conjugated ene-yne-ketene functionalities

Nakatani, Kazuhiko,Isoe, Sachihiko,Maekawa, Satoshi,Saito, Isao

, p. 605 - 608 (2007/10/02)

Upon photoirradiation, diazoketone 1 was found to induce single strand cleavage of plasmid pBR322 DNA at concentration of 100 μM. Conjugate ene-yne moiety was essential for DNA-cleaving activities.

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