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1-Chloro-2-pentafluorosulfanylcyclohexane is a complex organic chemical compound with the molecular formula C6H8ClF5S. It features a cyclohexane ring, which is a six-carbon saturated hydrocarbon ring, with a chlorine atom attached to one carbon and a pentafluorosulfanyl group (SF5) attached to another carbon. The pentafluorosulfanyl group is a highly electronegative and stable moiety, making the compound potentially useful in various chemical reactions and applications. Due to its unique structure and properties, 1-chloro-2-pentafluorosulfanylcyclohexane may be employed in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. However, it is essential to handle 1-chloro-2-pentafluorosulfanylcyclohexane with care, as it may possess hazardous properties and require specific safety measures during its use and storage.

1692-53-1

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1692-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1692-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,9 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1692-53:
(6*1)+(5*6)+(4*9)+(3*2)+(2*5)+(1*3)=91
91 % 10 = 1
So 1692-53-1 is a valid CAS Registry Number.

1692-53-1Relevant academic research and scientific papers

New and convenient method for incorporation of pentafluorosulfanyl (SF5) substituents into aliphatic organic compounds

Ait-Mohand, Samia,Dolbier Jr., William R.

, p. 3013 - 3015 (2002)

(figure presented) Use of Et3B as a catalytic initiator allows the convenient, regiospecific, and highly stereoselective addition of SF5Cl in high yield to a variety of alkenes and alkynes.

A convenient and efficient method for incorporation of pentafluorosulfanyl (SF5) substituents into aliphatic compounds

Dolbier Jr., William R.,A?t-Mohand, Samia,Schertz, Tyler D.,Sergeeva, Tatiana A.,Cradlebaugh, Joseph A.,Mitani, Akira,Gard, Gary L.,Winter, Rolf W.,Thrasher, Joseph S.

, p. 1302 - 1310 (2008/09/17)

Both SF5Cl and SF5Br undergo smooth, high yield addition to alkenes and alkynes under the mild free radical chain reaction conditions of triethylborane initiation at low temperature, although the SF5Br chemistry is somewha

Synthesis of SF5-benzene (SF5C6 H5 by the SF5-halide method

Winter, Rolf W.,Gard, Gary L.

, p. 549 - 552 (2007/10/03)

Several significant and useful syntheses of pentafluorothiobenzene (SF5C6H5) from SF5-halides (SF5X, X=Cl, Br) and cyclohexene or derivatives of cyclohexene are presented.

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