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L-Sorbose 1,6-bis(phosphate) is a chemical compound with the molecular formula C6H14O10P2. It is a phosphorylated derivative of L-sorbose, a sugar alcohol that is an isomer of glucose. L-Sorbose 1,6-bis(phosphate) plays a significant role in the Calvin cycle, a series of biochemical reactions that occur in plants, algae, and some bacteria, where it acts as an intermediate in the process of carbon fixation. L-Sorbose 1,6-bis(phosphate) is involved in the conversion of ribulose-1,5-bisphosphate into two molecules of 3-phosphoglycerate, which are then used to synthesize glucose and other sugars. The compound is also of interest in biochemistry and metabolic research due to its involvement in these essential metabolic pathways.

6915-27-1

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6915-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6915-27-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6915-27:
(6*6)+(5*9)+(4*1)+(3*5)+(2*2)+(1*7)=111
111 % 10 = 1
So 6915-27-1 is a valid CAS Registry Number.

6915-27-1Downstream Products

6915-27-1Relevant academic research and scientific papers

Synthesis of Sugars by Aldolase-Catalyzed Condensation Reactions

Wong, Chi-Huey,Whitesides, George M.

, p. 3199 - 3205 (1983)

Dihydroxyacetone phosphate was prepared in 200-mmol scale from dihydroxyacetone by two procedures: reaction with phosphorus oxytrichloride and glycerol kinase catalyzed phosphorylation using ATP with in situ regeneration of ATP by phosphoenolpyruvate or acetyl phosphate.Dihydroxyacetone phosphate was converted to fructose 6-phosphate in 80percent yield by exposure to a mixture of co-immobilized triosephosphate isomerase and aldolase followed by acid hydrolysis of the condensation product fructose 1,6-bisphosphate.Fructose 6-phosphate was subsequently converted by chemical and enzymatic schemes into fructose, glucose 6-phosphate, and glucose.Practical procedures are described for the preparation of D- and L-glyceraldehyde 3-phosphate and for several hexoses labeled with 13C in the C-2 and C-2,5 positions.

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