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4277-64-9

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4277-64-9 Usage

General Description

Ethyl 1H-pyrrole-1-carboxylate is a chemical compound with the molecular formula C7H9NO2. It is a derivative of pyrrole, a five-membered aromatic ring with one nitrogen atom. ethyl 1H-pyrrole-1-carboxylate is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. It is also used as a precursor for the synthesis of dyes and pigments. Ethyl 1H-pyrrole-1-carboxylate is known for its use in the development of drugs due to its ability to interact with biological systems. Its versatile nature and reactivity make it a valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 4277-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4277-64:
(6*4)+(5*2)+(4*7)+(3*7)+(2*6)+(1*4)=99
99 % 10 = 9
So 4277-64-9 is a valid CAS Registry Number.

4277-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl pyrrole-1-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-pyrrolecarboxylate

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:4277-64-9 SDS

4277-64-9Relevant articles and documents

The synthesis of the N-ethoxycarbonyl derivative of 5-azabicyclo[2.1.0]-pent-2-ene (Dewar pyrrole) - The first member of the parent ring-system

Warrener, Ronald N.,Amarasekara, Ananda S.,Russell, Richard A.

, p. 1519 - 1520 (2007/10/03)

N-Ethoxycarbonyl Dewar pyrrole 9, the first member of the parent ring, is formed via photofragmentation of 6 at -60°C and trapped as its adduct with 1,3-diphenylisobenzofuran 11; above this temperature, 9 is unstable and isomerises to N-ethoxycarbonylpyrrole 10.

ARE THIOPHENES ATTACKED AT SULPHUR BY NITRENES?

Meth-Cohn, Otto,Vuuren, Gerda van

, p. 1105 - 1108 (2007/10/02)

Ethyl azidoformate is shown to attack a range of thiophenes at sulphur giving transient S,N-ylides which can be trapped with acenaphthylene as adducts; thiophene yields self-trapped products also.

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