Cas 502927-16-4,(S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ<sup>6</sup>-thia-4-aza-tricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-propan-1-one

502927-16-4

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Product Name: (S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one
Synonyms:
CAS NO:502927-16-4
Molecular Formula:
Molecular Weight: 637.956
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: (S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(502927-16-4)
EPA Substance Registry System: (S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-diphenyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one(502927-16-4)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 502927-16-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 502927-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,9,2 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 502927-16:
(8*5)+(7*0)+(6*2)+(5*9)+(4*2)+(3*7)+(2*1)+(1*6)=134
134 % 10 = 4
So 502927-16-4 is a valid CAS Registry Number.

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502927-16-4Relevant academic research and scientific papers

A nucleophilic addition ring closure [NARC]-based synthesis of (+) -nonactic acid

Fraser, Benjamin,Perlmutter, Patrick

, p. 2896 - 2899 (2007/10/03)

Nonactic acid 1 has been synthesized in 12 steps from readily available (S)-(-)-ethyl lactate in 20% overall yield. The key ("NARC") sequence in this method involved anti-aldol addition of acylsultam 3 with aldehyde 4 followed by intramolecular oxymercura

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