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(2S,3E,5S)-1,2,5,6-tetrahydroxy-hex-3-ene is a complex organic compound characterized by its unique molecular structure. This chiral molecule features four hydroxyl groups (-OH) attached to carbons 1, 2, 5, and 6, with the double bond (C=C) located between carbons 3 and 4. The stereochemistry is specified by the (2S,3E,5S) notation, indicating the spatial arrangement of the hydroxyl groups on the chiral carbons. The "S" configuration at carbons 2 and 5 means that the hydroxyl groups are on the left side when looking at the molecule from the perspective of the priority of the substituents. The "E" configuration at carbon 3 indicates that the highest priority substituents (in this case, the hydroxyl groups) are on opposite sides of the double bond. (2S,3E,5S)-1,2,5,6-tetrahydroxy-hex-3-ene is of interest in the field of organic chemistry, particularly in the study of chiral molecules and their applications in pharmaceuticals and natural products.

6027-47-0

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6027-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6027-47-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6027-47:
(6*6)+(5*0)+(4*2)+(3*7)+(2*4)+(1*7)=80
80 % 10 = 0
So 6027-47-0 is a valid CAS Registry Number.

6027-47-0Relevant academic research and scientific papers

SYNTHESIS OF 1,2:5,6-DIANHYDRO-3,4-DIDEOXY-erythro- AND -D-threo-HEXITOL AND THEIR E-3-ENE DERIVATIVES

Kuszmann, Janos,Sohar, Pal

, p. 63 - 72 (2007/10/02)

Starting from 1,2:5,6-di-O-isopropylidene-D-mannitol and -D-glucitol, respectively, D-threo- and erythro-hex-E-3-enitol were synthesized: these were hydrogenated to the 3,4-dideoxy compounds, which were converted into the corresponding 1,2:5,6-dianhydride

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