Cas 262852-23-3,ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate

262852-23-3

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Basic information

Product Name: ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate
Synonyms: ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate
CAS NO:262852-23-3
Molecular Formula:
Molecular Weight: 390.393
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: ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate(262852-23-3)
EPA Substance Registry System: ethyl 6-deoxy-6-diazo-1,2-O-isopropylidene-3-O-(benzyl)-α-D-xylo-hept-5-ulofuranuronate(262852-23-3)

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: 262852-23-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 262852-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,8,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 262852-23:
(8*2)+(7*6)+(6*2)+(5*8)+(4*5)+(3*2)+(2*2)+(1*3)=143
143 % 10 = 3
So 262852-23-3 is a valid CAS Registry Number.

262852-23-3Upstream product

161144-16-7 ethyl-3-O-benzyl-6-deoxy-1,2-O-isopropylidene-α-D-xylo-heptofuranuronate-5-ulose

262852-23-3Downstream Products

262852-23-3Relevant academic research and scientific papers

An unusual observation in the rhodium carbenoids: [1,4]-migration in the sugar-derived α-diazo-β-ketoesters

Desai, Vijaya N.,Saha, Nabendu N.,Dhavale, Dilip D.

, p. 147 - 151 (2000)

In competition with [1,2]-migration, [2,3]-sigmatropic rearrangement and C-H insertion, product formation via an unusual [1,4]-migration is also found to be a prominent process in the rhodium carbenoids derived from sugar α-diazo-β-keto esters 2a-d. The R

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