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CAS

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226930-26-3

4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 226930-26-3 Structure

  • Basic information

    1. Product Name: 4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER
    2. Synonyms: 4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER
    3. CAS NO:226930-26-3
    4. Molecular Formula: C17H15NO2
    5. Molecular Weight: 265.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 226930-26-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER(226930-26-3)
    11. EPA Substance Registry System: 4-(1-NAPHTHALENYL)-1H-PYRROLE-3-CARBOXYLIC ACID ETHYL ESTER(226930-26-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 226930-26-3(Hazardous Substances Data)

226930-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226930-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,3 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 226930-26:
(8*2)+(7*2)+(6*6)+(5*9)+(4*3)+(3*0)+(2*2)+(1*6)=133
133 % 10 = 3
So 226930-26-3 is a valid CAS Registry Number.

226930-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-naphthalen-1-yl-1H-pyrrole-3-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:226930-26-3 SDS

226930-26-3Relevant articles and documents

Practical one-pot syntheses of ethyl 4-substituted-1 H-pyrrole-3- carboxylates from aldehydes

Chang, Jay Hyok,Shin, Hyunik

, p. 291 - 293 (2013/01/03)

Ethyl 4-substituted-1H-pyrrole-3-carboxylates were prepared in a one-pot manner starting from aromatic or aliphatic aldehydes via a Horner-Wadsworth- Emmons reaction and subsequent reaction with tosylmethylisocyanide (TosMIC) in the presence of sodium tert-amylate in toluene. Judicious selection of base and solvent led to the use of a single solvent, i.e., toluene, for reactions as well as for crystallization to render the one-pot process more practical and greener than the stepwise version. hisin@ lels.com.

Farnesyl transferase inhibitors having a piperidine structure and process for preparation thereof

-

, (2008/06/13)

The present invention relates to a novel piperidine derivative represented by formula (1) which shows an inhibitory activity against farnesyl transferase or pharmaceutically acceptable salts thereof, in which A, E and G are defined in the specification; t

A novel class of highly potent, selective, and non-peptidic inhibitor of ras farnesyltransferase (FTase)

Lee, Hyunil,Lee, Jinho,Lee, Sangkyun,Shin, Youseung,Jung, Wonhee,Kim, Jong-Hyun,Park, Kiwon,Kim, Kwihwa,Cho, Heung Soo,Ro, Seonggu,Lee, Sunhwa,Jeong, ShinWu,Choi, Taesaeng,Chung, Hyun-Ho,Koh, Jong Sung

, p. 3069 - 3072 (2007/10/03)

Design, synthesis and structure-activity relationship of a class of aryl pyrroles as farnesyltransferase inhibitors are described. In vitro and in vivo evaluation of a panel of these inhibitors led to identification of 2 (LB42908) as a highly potent (IC50=0.9 nM against H-Ras and 2.4 nM against K-Ras) antitumor agent that is currently undergoing preclinical studies.

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