Cas 1256356-03-2,(5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone

1256356-03-2

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Basic information

Product Name: (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone
Synonyms: (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone
CAS NO:1256356-03-2
Molecular Formula:
Molecular Weight: 514.737
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: (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone(CAS DataBase Reference)
NIST Chemistry Reference: (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone(1256356-03-2)
EPA Substance Registry System: (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-(4-methoxybenzyloxymethyl)cyclohex-2-enone(1256356-03-2)

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: 1256356-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256356-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1256356-03:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*6)+(2*0)+(1*3)=152
152 % 10 = 2
So 1256356-03-2 is a valid CAS Registry Number.

1256356-03-2Upstream product

1256356-03-2Downstream Products

1256356-04-3 (5R,6R)-6-(tert-butyldiphenylsilanyloxymethyl)-5-hydroxymethylcyclohex-2-enone

1256356-03-2Relevant academic research and scientific papers

Asymmetric synthesis of hydroxy-skipped bishomo-inositols as potential glycosidase inhibitors

Mahapatra, Tridib,Nanda, Samik

experimental part, p. 2199 - 2205 (2010/11/04)

Four isomeric hydroxy-skipped bishomo-inositol analogs have been synthesized from both enantiomers of 5-hydroxymethyl-2-cyclohexenone. Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylation are the key reactions which have

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