17107-32-3 Usage
Family
Polyhydroxylated alcohols
Type
Synthetic organic compound
Derivative of
D-mannitol
Two bromine atoms
Attached to carbon atoms at positions 1 and 6
Isopropylidene group
Present at positions 3 and 4
Organic synthesis
Used in the synthesis of various chemical compounds
Medicinal chemistry
Utilized in the development of pharmaceutical agents
Building block
Serves as a valuable component for creating other important chemical compounds in the lab
Check Digit Verification of cas no
The CAS Registry Mumber 17107-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17107-32:
(7*1)+(6*7)+(5*1)+(4*0)+(3*7)+(2*3)+(1*2)=83
83 % 10 = 3
So 17107-32-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H16Br2O4/c1-7(2)8(14,5(12)3-10)9(7,15)6(13)4-11/h5-6,12-15H,3-4H2,1-2H3
17107-32-3Relevant academic research and scientific papers
Solvent-free organic reactions on silica gel supports. Facile transformation of epoxides to β-halohydrins with lithium halides
Kotsuki, Hiyoshizo,Shimanouchi, Tomoyasu,Ohshima, Reiji,Fujiwara, Shunsuke
, p. 2709 - 2722 (2007/10/03)
The reaction of epoxides with lithium halides was efficiently promoted on the surface of silica gel in the absence of any solvent to give the corresponding β-halohydrins. The reactivity of lithium halides was shown to follow the order LiI > LiBr >> LiCl, and the reactivity of LiCl was dramatically increased by adding an equivalent amount of water to this system. On the other hand a similar reaction with α,β-epoxyketones produces the α-haloenone derivatives, presumably via halohydrin intermediates. The epoxide-opening reaction of (R)-(+)-styrene oxide was also investigated to clarify the stereochemical features of this reaction.
