Cas 885703-65-1,(E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one

885703-65-1

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Basic information

Product Name: (E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one
Synonyms: (E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one
CAS NO:885703-65-1
Molecular Formula:
Molecular Weight: 465.753
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: (E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one(885703-65-1)
EPA Substance Registry System: (E)-(2S,3R)-1-((S)-4-Benzyl-2-thioxo-thiazolidin-3-yl)-6-(tert-butyl-dimethyl-silanyloxy)-3-hydroxy-2-methyl-hex-4-en-1-one(885703-65-1)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 885703-65-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 885703-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,7,0 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 885703-65:
(8*8)+(7*8)+(6*5)+(5*7)+(4*0)+(3*3)+(2*6)+(1*5)=211
211 % 10 = 1
So 885703-65-1 is a valid CAS Registry Number.

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885703-65-1Relevant academic research and scientific papers

Enantioselective total synthesis of FD-891

Crimmins, Michael T.,Caussanel, Franck

, p. 3128 - 3129 (2006)

The enantioselective synthesis of FD-891 has been achieved with a longest linear sequence of 21 steps. The synthetic strategy involves the use of aldol additions of a chlorotitanium enolate of N-acylthiazolidinethiones as the key reaction to establish 6 o

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