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1421373-36-5

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  • 3-chloro-N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxy-5-(4-(1-methyl-1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)propanamid

    Cas No: 1421373-36-5

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  • 3-chloro-N-[2-[2-dimethylaminoethyl(methyl)amino]-4-methoxy-5-[[4-(1-methylindol-3-yl)pyrimidin-2-yl]amino]phenyl]propanamide

    Cas No: 1421373-36-5

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1421373-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421373-36-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,3,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1421373-36:
(9*1)+(8*4)+(7*2)+(6*1)+(5*3)+(4*7)+(3*3)+(2*3)+(1*6)=125
125 % 10 = 5
So 1421373-36-5 is a valid CAS Registry Number.

1421373-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-N-[2-[2-dimethylaminoethyl(methyl)amino]-4-methoxy-5-[[4-(1-methylindol-3-yl)pyrimidin-2-yl]amino]phenyl]propanamide

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:1421373-36-5 SDS

1421373-36-5Relevant articles and documents

Preparation method of antitumor drug AZD9291

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Paragraph 0030, (2018/07/30)

The invention relates to a preparation method of an antitumor drug AZD9291. The preparation method comprises the following steps: taking 2-bromo-4-anisidine as a starting raw material; carrying out nitration reaction, grignard reaction, acylation reaction, reduction reaction, grignard reaction and elimination reaction to obtain AZD9291 free alkali. The preparation method disclosed by the inventionhas the beneficial effects of wide source of raw materials, low cost, simple operation, recyclable application of a solvent, low discharge amount of waste liquid, high recovery rate of a product andthe like, and easily realizes industralization.

Preparation method for osimertinib

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Paragraph 0028; 0029; 0033; 0034; 0038; 0039; 0043; 0044, (2018/01/17)

The invention provides a preparation method for osimertinib. According to the invention, the raw material 3-chloropropionic acid has low toxicity and stable properties and is easily available; reaction conditions are mild; operation is simple; high-yield high-purity osimertinib can be prepared; and the method is suitable for industrial production.

2 - (2, 4, 5 - SUBSTITUTED -ANILINO) PYRIMIDINE DERIVATIVES AS EGFR MODULATORS USEFUL FOR TREATING CANCER

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, (2013/03/26)

The present invention relates to certain 2-(2,4,5-substituted-anilino) pyrimidine compounds and pharmaceutically acceptable salts thereof which may be useful in the treatment or prevention of a disease or medical condition mediated through certain mutated forms of epidermal growth factor receptor (for example the L858R activating mutant, the Exonl9 deletion activating mutant and the T790M resistance mutant). Such compounds and salts thereof may be useful in the treatment or prevention of a number of different cancers. The invention also relates to pharmaceutical compositions comprising said compounds and salts thereof, especially useful polymorphic forms of these compounds and salts, intermediates useful in the manufacture of said compounds and to methods of treatment of diseases mediated by various different forms of EGFR using said compounds and salts thereof.

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