Cas 255384-97-5,dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate

255384-97-5

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Basic information

Product Name: dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate
Synonyms: dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate
CAS NO:255384-97-5
Molecular Formula:
Molecular Weight: 418.427
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate(255384-97-5)
EPA Substance Registry System: dibenzyl (4R)-(4,5-dihydroxy-4,5-O-isopropylidene-3-oxopentyl)phosphonate(255384-97-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 255384-97-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 255384-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,3,8 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 255384-97:
(8*2)+(7*5)+(6*5)+(5*3)+(4*8)+(3*4)+(2*9)+(1*7)=165
165 % 10 = 5
So 255384-97-5 is a valid CAS Registry Number.

255384-97-5Upstream product

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255384-97-5Relevant academic research and scientific papers

Origin of the slow-binding inhibition of aldolase by D-glycero-tetrulose 1-phosphate (D-erythrulose 1-phosphate) from the comparison with the isosteric phosphonate analog

Page, Patrick,Blonski, Casimir,Périé, Jacques

, p. 2853 - 2857 (1999)

The mechanistic reaction pathway for the slow-binding inhibition of rabbit muscle aldolase by D-glycero-tetrulose 1-phosphate (D-erythrulose 1- phosphate) was investigated through the use of its phosphonomethyl isoster 4 which was synthezised for this stu

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