Cas 127760-56-9,(1R,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol

127760-56-9

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Basic information

Product Name: (1R,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol
Synonyms:
CAS NO:127760-56-9
Molecular Formula:
Molecular Weight: 608.968
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: (1R,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol(127760-56-9)
EPA Substance Registry System: (1R,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol(127760-56-9)

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: 127760-56-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127760-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,7,6 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127760-56:
(8*1)+(7*2)+(6*7)+(5*7)+(4*6)+(3*0)+(2*5)+(1*6)=139
139 % 10 = 9
So 127760-56-9 is a valid CAS Registry Number.

127760-56-9Upstream product

127696-06-4 (2S-trans)-2,3-bis[(t-butyldiphenylsilyloxy)methyl]-cyclobutanone

127760-56-9Downstream Products

127696-07-5 (1S,2S,3S)-2,3-Bis-(tert-butyl-diphenyl-silanyloxymethyl)-cyclobutanol

127760-56-9Relevant academic research and scientific papers

Enantio- and Diastereo-selective Synthesis of Carbocyclic Oxetanocin Analogues

Ichikawa, Yuh-ichiro,Narita, Aya,Shiozawa, Akira,Hayashi, Yujiro,Narasaka, Koichi

, p. 1919 - 1921 (1989)

Carbocyclic oxetanocin-A (COXT-A) (2a) and -G (COTX-G) (2b) were synthesised enantio- and diastereo-selectively; these compounds exhibited potent antiviral activities.

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