Cas 1256355-98-2,(2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone

1256355-98-2

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Basic information

Product Name: (2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone
Synonyms: (2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone
CAS NO:1256355-98-2
Molecular Formula:
Molecular Weight: 428.601
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: (2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone(1256355-98-2)
EPA Substance Registry System: (2S,3S,5R,6R)-2-(tert-butyldiphenylsilanyloxymethyl)-5,6-dihydroxy-3-hydroxymethylcyclohexanone(1256355-98-2)

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: 1256355-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256355-98-2 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 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-98:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*9)+(1*8)=172
172 % 10 = 2
So 1256355-98-2 is a valid CAS Registry Number.

1256355-98-2Upstream product

1256355-97-1 (5S,6S)-6-(tert-butyldiphenylsilanyloxymethyl)-5-hydroxymethylcyclohex-2-enone

1256355-98-2Downstream Products

1334017-20-7 C₂₄H₃₄O₅Si

1256355-98-2Relevant 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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