Cas 1060710-03-3,(1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde

1060710-03-3

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Basic information

Product Name: (1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde
Synonyms: (1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde
CAS NO:1060710-03-3
Molecular Formula:
Molecular Weight: 534.652
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: (1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde(1060710-03-3)
EPA Substance Registry System: (1S,2R,3R,4R)-2,3,5-Tris-benzyloxy-4-hydroxy-6-[1-phenyl-meth-(Z)-ylidene]-cyclohexanecarbaldehyde(1060710-03-3)

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: 1060710-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1060710-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,7,1 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1060710-03:
(9*1)+(8*0)+(7*6)+(6*0)+(5*7)+(4*1)+(3*0)+(2*0)+(1*3)=93
93 % 10 = 3
So 1060710-03-3 is a valid CAS Registry Number.

1060710-03-3Upstream product

1060710-03-3Downstream Products

1060754-09-7 (1R,2R,3R,4R)-2,3,6-Tris-benzyloxy-4-hydroxymethyl-5-[1-phenyl-meth-(Z)-ylidene]-cyclohexanol

1060710-03-3Relevant academic research and scientific papers

A Divergent Route for a Total Synthesis of Cyclophellitol and Epicyclophellitol from a Oxabicyclic Glycoside Prepared from D-Glucal

McDevitt, R. E.,Fraser-Reid, B.

, p. 3250 - 3252 (2007/10/02)

D-Glucal has been used for syntheses of Tatsuta's penultimate intermediate for cyclophellitol and epicyclophellitol via a 6-exo-trig radical cyclization of 2-deoxy-2-iodo-6-alkynyl glycoside, the diastereomeric mixture produced thereby being separated into two sets, each of which leads to one or other target materials.

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