16656-02-3 Usage
Description
D-glycero-D-altro-octulose 1,8-bisphosphate is a ketooctose derivative that is D-glycero-D-altro-octulose carrying two phosphate substituents at positions 1 and 8. It is a unique carbohydrate molecule with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
D-glycero-D-altro-octulose 1,8-bisphosphate is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure and phosphate groups may offer novel mechanisms of action and therapeutic benefits in the treatment of various diseases.
Used in Chemical Research:
D-glycero-D-altro-octulose 1,8-bisphosphate is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studying carbohydrate chemistry, enzymatic reactions, and other related processes.
Used in Biochemical Studies:
D-glycero-D-altro-octulose 1,8-bisphosphate is used as a biochemical tool for investigating metabolic pathways and enzyme mechanisms. Its presence in certain metabolic pathways may provide insights into the regulation and function of these processes.
Used in Analytical Chemistry:
D-glycero-D-altro-octulose 1,8-bisphosphate is used as an analytical standard in the development and validation of analytical methods for the detection and quantification of carbohydrates and their derivatives.
Used in Material Science:
D-glycero-D-altro-octulose 1,8-bisphosphate may have potential applications in material science, such as the development of new materials with unique properties based on its structure and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 16656-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,5 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16656-02:
(7*1)+(6*6)+(5*6)+(4*5)+(3*6)+(2*0)+(1*2)=113
113 % 10 = 3
So 16656-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O14P2/c9-3(1-21-23(15,16)17)5(11)7(13)8(14)6(12)4(10)2-22-24(18,19)20/h3,5-9,11-14H,1-2H2,(H2,15,16,17)(H2,18,19,20)/t3-,5+,6+,7+,8-/m0/s1
16656-02-3Relevant articles and documents
IMPROVED METHODS FOR THE ENZYMIC PREPARATION AND CHROMATOGRAPHY OF OCTULOSE PHOSPHATES
Kapuscinski, Mirek,Franke, Fritz P.,Flanigan, Ian,MacLeod, John K.,Williams, John F.
, p. 69 - 80 (1985)
High-yield methods are presented for the synthesis of D-glycero-D-altro-octulose 8-phosphate and 1,8-diphoshate, and D-glycero-ido-octulose 1,8-diphosphate and 8-phosphate.Formate ion-exchange and DEAE-Sephadex A-25 borate column chromatography were used for the isolation of these compounds.A new phenylboronate-containing solvent for p.c. and t.l.c. of sugar phosphates is described.The 13C-n.m.r. assignments of the major contributing structure of D-glycero-D-altro-octulose 8-phosphate in aqueous solution (pH 7.0) are presented.
