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diethyl 1-aMino-3-ethyl-1H-pyrrole-2,4-dicarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

869066-98-8

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869066-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869066-98-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,0,6 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 869066-98:
(8*8)+(7*6)+(6*9)+(5*0)+(4*6)+(3*6)+(2*9)+(1*8)=228
228 % 10 = 8
So 869066-98-8 is a valid CAS Registry Number.

869066-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 1-amino-3-ethylpyrrole-2,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names DIETHYL 1-AMINO-3-ETHYL-1H-PYRROLE-2,4-DICARBOXYLATE

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:869066-98-8 SDS

869066-98-8Relevant academic research and scientific papers

An efficient electrophilic N-amination utilizing in situ generated chloramine under phase transfer conditions

Bhattacharya, Apurba,Patel, Nitin C.,Plata, Robert Erik,Peddicord, Michael,Ye, Qingmei,Parlanti, Luca,Palaniswamy, Venkatapuram A.,Grosso, John A.

, p. 5341 - 5343 (2007/10/03)

An efficient, one-pot, phase transfer N-amination technology was developed. The protocol utilizes chloramine, an inexpensive and safe electrophilic aminating agent potentially viable for commercial manufacturing.

New dual inhibitors of EGFR and HER2 protein tyrosine kinases

Fink, Brian E.,Vite, Gregory D.,Mastalerz, Harold,Kadow, John F.,Kim, Soong-Hoon,Leavitt, Kenneth J.,Du, Karen,Crews, Donald,Mitt, Toomas,Wong, Tai W.,Hunt, John T.,Vyas, Dolatrai M.,Tokarski, John S.

, p. 4774 - 4779 (2007/10/03)

A novel series of dual EGFR and HER2 inhibitors based on the pyrrolo[2,1-f][1,2,4]triazine nucleus is described. A general route toward their synthesis, which enables functionalization at multiple sites, has been developed. Biological evaluation in enzyma

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