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(+/-)-1,2-O-isopropylidene-myo-inositol is a chemical compound derived from myo-inositol, a naturally occurring sugar alcohol found in various fruits, beans, and whole grains. (+/-)-1,2-O-isopropylidene-myo-inositol is formed by the acetal protection of the hydroxyl groups at the 1 and 2 positions of myo-inositol, using isopropylidene (2,2-dimethyl-1,3-dioxolane) as the protecting group. The resulting product is a cyclic acetal, which is often used in organic synthesis as a protecting group for diols, particularly in the preparation of complex carbohydrates and other biologically active compounds. The (+/-) notation indicates that the compound exists as a racemic mixture, containing equal amounts of both the R and S enantiomers.

6404-82-6

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6404-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6404-82-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6404-82:
(6*6)+(5*4)+(4*0)+(3*4)+(2*8)+(1*2)=86
86 % 10 = 6
So 6404-82-6 is a valid CAS Registry Number.

6404-82-6Upstream product

6404-82-6Relevant academic research and scientific papers

Synthesis of all possible regioisomers of myo-inositol pentakisphosphate

Chung, Sung-Kee,Chang, Young-Tae

, p. 2039 - 2042 (2007/10/03)

Synthesis of all possible 4 regioisomers of IP5, naturally occurring metabolites of IP3 and IP4, was accomplished from myo-inositol via its monobenzoate derivatives (IBz1) as the key intermediates; base-catalyzed isomerization of readily available IBz1 derivatives, followed by suitable separation procedures efficiently provided the requisite regioisomers of IBz1.

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