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1-bromo-2-cyclopropylmethoxy-4-fluoro-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1173006-34-2

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1173006-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1173006-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,0,0 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1173006-34:
(9*1)+(8*1)+(7*7)+(6*3)+(5*0)+(4*0)+(3*6)+(2*3)+(1*4)=112
112 % 10 = 2
So 1173006-34-2 is a valid CAS Registry Number.

1173006-34-2Downstream Products

1173006-34-2Relevant academic research and scientific papers

METHYLPYRROLOPYRIMIDINECARBOXAMIDES

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Page/Page column 104, (2012/06/18)

The compounds of Formula (I), wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.

METHYLPYRROLOPYRIMIDINECARBOXAMIDES

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Page/Page column 167-168, (2011/04/14)

The compounds of formula (I) wherein R1, R2, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, and the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiestera

METHYLPYRROLOPYRIDINECARBOXAMIDES

-

Page/Page column 86, (2011/04/14)

The compounds of formula (I) wherein R1, R21, R22, R23, R24, Y and R3 have the meanings as given in the description, the salts thereof, and the stereoisomers of the compounds and the salts thereof are effective inhibitors of the type 5 phosphodiesterase.

Regioselective SNAr reactions of substituted difluorobenzene derivatives: practical synthesis of fluoroaryl ethers and substituted resorcinols

Ouellet, Stéphane G.,Bernardi, Anna,Angelaud, Remy,O'Shea, Paul D.

supporting information; experimental part, p. 3776 - 3779 (2009/10/11)

In this Letter, we describe a practical and highly selective method for the preparation of fluoroaryl ethers and differentially substituted resorcinol derivatives. This synthetic strategy relies on a selective SNAr of substituted difluorobenzen

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