Cas 129753-00-0,1-[(1R,2R,3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2-fluoro-4-thiocyanato-cyclopentyl]-3-((E)-3-methoxy-2-methyl-acryloyl)-urea

129753-00-0

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Basic information

Product Name: 1-[(1R,2R,3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2-fluoro-4-thiocyanato-cyclopentyl]-3-((E)-3-methoxy-2-methyl-acryloyl)-urea
Synonyms:
CAS NO:129753-00-0
Molecular Formula:
Molecular Weight: 569.772
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: 1-[(1R,2R,3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2-fluoro-4-thiocyanato-cyclopentyl]-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(1R,2R,3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2-fluoro-4-thiocyanato-cyclopentyl]-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(129753-00-0)
EPA Substance Registry System: 1-[(1R,2R,3R,4R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-2-fluoro-4-thiocyanato-cyclopentyl]-3-((E)-3-methoxy-2-methyl-acryloyl)-urea(129753-00-0)

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: 129753-00-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129753-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 129753-00:
(8*1)+(7*2)+(6*9)+(5*7)+(4*5)+(3*3)+(2*0)+(1*0)=140
140 % 10 = 0
So 129753-00-0 is a valid CAS Registry Number.

129753-00-0Upstream product

540-72-7 sodium thiocyanide

129753-00-0Downstream Products

129753-00-0Relevant academic research and scientific papers

Preparation of Optically Active 6'-Fluorocarbocyclic Nucleosides utilising an Enantiospecific Enzyme-catalysed Baeyer-Villiger Type Oxidation

Levitt, Melissa S.,Newton, Roger F.,Roberts, Stanley M.,Willetts, Andrew J.

, p. 619 - 620 (1990)

Kinetic resolution of the racemic ketone (+/-)-(1) was achieved using Acinetobacter NCIB 9871: the optically active norbornanone was converted into the carbocyclic nucleosides (5) and (7).

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