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D-2,5-hexodiulose 1-phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16808-78-9

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16808-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16808-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,0 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16808-78:
(7*1)+(6*6)+(5*8)+(4*0)+(3*8)+(2*7)+(1*8)=129
129 % 10 = 9
So 16808-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11O9P/c7-1-3(8)5(10)6(11)4(9)2-15-16(12,13)14/h5-7,10-11H,1-2H2,(H2,12,13,14)/t5-,6-/m1/s1

16808-78-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S,4S)-3,4,6-trihydroxy-2,5-dioxohexyl] dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names D-threo-2,5-hexodiulose 1-phosphate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:16808-78-9 SDS

16808-78-9Upstream product

16808-78-9Downstream Products

16808-78-9Relevant academic research and scientific papers

STRUCTURES OF D-THREO-2,5-HEXODIULOSE 1-PHOSPHATE AND D-THREO-2,5-HEXODIULOSE 1,6-BIPHOSPHATE (5-KETO-D-FRUCTOSE MONO- AND BIS-PHOSPHATE) IN SOLUTION BY 13C-N.M.R. SPECTROSCOPY

Butera, Loredana,Englard, Sasha,Blanchard, John S.,Avigad, Gad

, p. 179 - 188 (2007/10/02)

The mono- (2) and bis-phosphate (3) derivatives of D-threo-2,5-hexodiulose (1) (5-keto-D-fructose) were synthesized enzymically and purified by anion-exchange chromatography.The proportions, sizes of ring, and anomeric configurations were determined by F.t. 31P- and 13C-n.m.r. spectroscopy.Compound 2 was found to exist preponderantly (70-78percent) in the β-pyranose form with the remainder existing in the 2R,5R-furanose form.Compound 3 assumes two different furanose forms in solution, one (77-84percent) being the 2R,5R-furanose form and the other the 2S,5R-furanose form.

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