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(S)-(-)-3,4-difluoro-2-[2-(2-tetrahydropyranyloxy)propoxy]nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

124410-01-1

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124410-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124410-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,1 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124410-01:
(8*1)+(7*2)+(6*4)+(5*4)+(4*1)+(3*0)+(2*0)+(1*1)=71
71 % 10 = 1
So 124410-01-1 is a valid CAS Registry Number.

124410-01-1Relevant articles and documents

Propoxybenzene derivatives and process for preparing the same

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, (2008/06/13)

Propoxybenzene derivatives represented by the following formula STR1 wherein Ra represents a nitro group, an amino group which may have a protecting group or an --NHCH=C(COO--C1-6 -Alkyl)2 group, Rb represents a hydrogen atom, a protecting group for the hydroxyl group or a substituted sulfonyl group and Xa and Xb, which may be the same or different, each represents a halogen atom, and processes for preparation thereof are disclosed. These derivatives are useful in preparing antibacterial agents.

Optically active benzoxazines and bezothiazines and a process for their stereospecific preparation

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, (2008/06/13)

Optically active 7,8-difluoro-3,4-dihydro-3--methyl-2H-[1,4]benzoxazines and 7,8-difluoro-3,4-dihydro-2--methyl-2H-[1,4]benzoxazines and the corresponding benzothiazines of formula III, where, one of the substituents R1, R2, R3 and R4 is CH2OH or -CH2Z, the remaining being hydrogen, X denotes fluoro, chloro, methyl or hydrogen, Y is oxygen or sulfur and Z is hydrogen, fluoro or protected hydroxyl are obtained as the stereochemically pure products of a stereospecific synthesis using a 3,4-difluoronitrobenzene substituted with a stereochemically pure 2-(1-hydroxyisopropoxy), 2-(2--hydroxypropoxy), 2-(1-hydroxyisopropylthio) or 2-(2--hydroxypropylthio) substituent. The obtained compounds are suited for the production of optically active pyridobenzoxazines and pyridobenzothiazines, among which are useful antibacterial optically active quinolones, particularly (S)-(-)-ofloxacin.

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