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(S)-1-Bromo-3-fluoro-butane is a chiral organic compound with the molecular formula C4H7BrF. It is a colorless liquid at room temperature and has a distinct chemical structure, featuring a bromine atom at the first carbon and a fluorine atom at the third carbon in a butane chain. The "S" prefix indicates that it is the (S)-enantiomer, which means it has a specific spatial arrangement of atoms that is different from its (R)-enantiomer counterpart. (S)-1-Bromo-3-fluoro-butane is used in various chemical synthesis processes, particularly in the production of pharmaceuticals and agrochemicals, due to its unique reactivity and stereochemistry.

6089-10-7

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6089-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6089-10-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6089-10:
(6*6)+(5*0)+(4*8)+(3*9)+(2*1)+(1*0)=97
97 % 10 = 7
So 6089-10-7 is a valid CAS Registry Number.

6089-10-7Upstream product

6089-10-7Downstream Products

6089-10-7Relevant academic research and scientific papers

REACTIONS OF HALOGEN FLUORIDES. XI. MECHANISM OF REACTIONS OF ALKYL HALIDES WITH BROMINE TRIFLUORIDE

Kartashov, A. V.,Chuvatkin, N. N.,Kurskii, Yu. A.,Boguslavskaya, L. S.

, p. 2279 - 2284 (2007/10/02)

The effects of the substituted halogen, the neighboring groups, and the polarity of the medium on the nature of the fluorination products were studied for the reactions of δ-substituted halogenobutanes and 1,2,3-trihalogenobutanes with bromine tetrachloride.A mechanism involving formation of linear halogenonium ions at the rate-determining stage is proposed.

REACTIONS OF HALOGENS FLUORIDES. VIII. SUBSTITUTIVE FLUORINATION OF BROMINE-CONTAINING ALKANES AND ESTERS WITH BROMINE TRIFLUORIDE

Chuvatkin, N. N.,Kartashov, A. V.,Morozova, T. V.,Boguslavskaya, L. S.

, p. 237 - 242 (2007/10/02)

The conditions were found for selective liquid-phase substitutive fluorination of bromine-substituted alkanes and esters with pure bromine trifluoride, in which all three fluorine atoms of the BrF3 molecule are used effectively in the fluorination.The exchange of bromine for fluorine in monobromohalogenoalkanes is nonstereospecific and is in a number of cases accompanied by skeletal rearrangements, hydride shifts, and migration of the halogen.A carbocationic mechanism of fluorination is discussed.

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