Cas 1225501-48-3,2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime

1225501-48-3

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Basic information

Product Name: 2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime
Synonyms: 2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime
CAS NO:1225501-48-3
Molecular Formula:
Molecular Weight: 547.694
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: 2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime(CAS DataBase Reference)
NIST Chemistry Reference: 2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime(1225501-48-3)
EPA Substance Registry System: 2,3,4-tri-O-benzyl-5,6,7,8-tetradeoxy-D-xylo-oct-5(E),7-dienone O-benzyl-oxime(1225501-48-3)

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: 1225501-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1225501-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,5,0 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1225501-48:
(9*1)+(8*2)+(7*2)+(6*5)+(5*5)+(4*0)+(3*1)+(2*4)+(1*8)=113
113 % 10 = 3
So 1225501-48-3 is a valid CAS Registry Number.

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1225501-48-3Relevant academic research and scientific papers

Application of sugar allyltin derivatives for the preparation of heterocyclic compounds

Magdycz, Marta,Cmoch, Piotr,Jarosz, Sawomir

experimental part, p. 1303 - 1318 (2010/10/01)

Controlled fragmentation of sugar allyltin, derivative of D-glucose, provided the eight carbon atom synthon: (2R,3S,4R)-tris(benzyloxy)oct-5,7-diene, which was used for the preparation of complex heterocyclic compounds. First step involved formation of th

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