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Cyclopropanecarboxamide, N-methoxy-N,2-dimethyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

192644-20-5

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192644-20-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192644-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 192644-20:
(8*1)+(7*9)+(6*2)+(5*6)+(4*4)+(3*4)+(2*2)+(1*0)=145
145 % 10 = 5
So 192644-20-5 is a valid CAS Registry Number.

192644-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Methoxy-N,2-dimethylcyclopropanecarboxamide

1.2 Other means of identification

Product number -
Other names 2-Methylcyclohexylselencyanat

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:192644-20-5 SDS

192644-20-5Relevant academic research and scientific papers

CYCLOPROPYL ETHYLENE COMPOUND AND ARTHROPOD PEST CONTROL COMPOSITION CONTAINING SAME

-

Paragraph 0339-0342; 0345, (2021/02/05)

The present invention provides a compound that have excellent harmful arthropod controlling effects, the compounds being represented by formula (I) [wherein R1 represents a hydrogen atom etc., and R21, R22, R31

[...] compound pest control method (by machine translation)

-

Paragraph 0248-0250, (2020/01/02)

[A] a method for controlling harmful organisms. (I) formula [a][In the formula, R1 The, represents a hydrogen atom or the like, R21 , R22 , R31 , And R32 The, same or different, represents a hydrogen

Synthesis of chiral β-methyl tryptamine-derived GnRH antagonists

Simeone, Joseph P.,Bugianesi, Robert L.,Ponpipom, Mitree M.,Goulet, Mark T.,Levorse, Mark S.,Desai, Ranjit C.

, p. 6459 - 6461 (2007/10/03)

The stereospecific formation of 2-aryl-β-methyl tryptamine derivatives 15 and 16 from chiral 4-chloro-1-(3,5-dimethylphenyl)-3-methylbutanones is described. These intermediates were further manipulated into the GnRH antagonists 1b and 1c in five steps.

Antagonists of gonadotropin releasing hormone

-

, (2008/06/13)

There are disclosed compounds of formula (I) and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related and other conditions in both men and women.

ANTAGONISTS OF GONADOTROPIN RELEASING HORMONE

-

, (2008/06/13)

There are disclosed compounds of formula (I) STR1 and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related and other conditions in both men and women.

ANTAGONISTS OF GONADOTROPIN RELEASING HORMONE

-

, (2008/06/13)

There are disclosed compounds of formula (I) STR1 and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related and other conditions in both men and women.

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